Mutacin I biosynthesis genes and proteins

ABSTRACT

According to the present invention, an isolated and purified DNA sequence which encodes a lantibiotic, mutacin I, is disclosed. The nucleic acid sequence is set forth in SEQ ID No: 1 and the amino acid sequence is set forth in SEQ ID No: 2.

GRANT REFERENCE

[0001] The subject invention was made with government support under a grant from the National Institutes of Health (NIH RO 1 DE09082). The government has certain rights in the invention.

FIELD OF THE INVENTION

[0002] The invention relates to polypeptide antibiotics and to the identification of genetic loci associated with expression of the antibiotics. The invention particularly describes a purified lanthionine-containing antimicrobial agent, DNA encoding the protein, and methods and compositions for treatments employing the antibiotic.

BACKGROUND OF THE INVENTION

[0003] Several species of bacteria inhabit the human oral cavity; among them Streptococcus mutans is considered a major etiologic agent responsible for dental caries. Loesche (1986) Microbiol. Rev. 50:353-380. Previous studies showed a certain percentage of clinical isolates of S. mutans producing antimicrobial substances called mutacins. Caufield et al. (1985) Infect. Immun. 48:51-56; Hamada et al. (1975) Arch. Oral Biol. 20:641-648. Mutacins are active against closely related species as well as a surprisingly wide spectrum of other Gram-positive bacteria. Parrot et al. (1990) Can. J. Microbiol. 36:123-130. The ability to produce mutacins, combined with lactic acid production by S. mutans may contribute to the pathogenesis of these bacteria. Kleinberg, p. 605-624, in W. A. Nolte (ed.), Oral microbiology, The C.V. Mosby Company, St. Louis. Production of mutacins by S. mutans and other oral streptococci may also play a protective role to the host against pathogens such as Group A streptococci and Streptococcus pneumoniae. In this respect, mutacins may serve as antimicrobial agents in the future.

[0004] Lantibiotics are lanthionine-containing small peptide antibiotics that are produced by gram-positive bacteria. Jung (ed.), p. 1-34, in G. Jung and H. G. Sahl (ed.), Nisin and novel lantibiotics, ESCOM Sci. Publ., Leiden; Sahl et al. (1995) Eur. J. Biochem. 230:827-853. The lantibiotics are ribosomally synthesized and post-translationally modified. The modification reactions include dehydration of serine and threonine residues and the addition of thiol groups from cycteine residues to the double bound to form lanthionines and β-methyllanthionines, respectively. Some dehydrated serine or threonine may remain as such in the mature lantibiotic molecule.

[0005] Based on the secondary structures, Jung assigned lantibiotics into two classes, Type-A (linear) and Type-B (globular). Jung (ed.), p. 1-34, in G. Jung and H. G. Sahl (ed.), Nisin and novel lantibiotics, ESCOM Sci. Publ., Leiden. de Vos et al. ((1995) Molecular Microbiol. 17:427-437) and Sahl and Bierbaum (Sahl et al. (1998) Annu. Rev. Microbiol. 52:41-79) further divided each class into subgroups according to their primary peptide sequences. Thus, subgroup AI contains the nisin-like lantibiotics with nisin, subtilin, epidermin and pep5 as the most thoroughly characterized members. Allgaier et al. (1986) Eur. J. Biochem. 160:9-22; Gross et al. (1968) FEBS Lett. 2:61-64; Gross et al. (1971) J. Am. Chem. Soc. 93:4634-4635; Kaletta et al. (1989) Arch. Microbiol. 152:16-19; Well et al. (1990) Eur. J. Biochem. 194:217-223. Subgroup AII consists of lacticin 481, SA-FF22, salivaricin and variacin. Hynes et al. (1993) Appl. Environ. Microbiol. 59:1969-1971; Piard et al. (1993) J. Biol. Chem. 268:16361-16368; Pridmore et al. (1996) Appl. Environ. Microbiol 62:1799-1802; Ross et al. (1993) Appl. Environ. Microbiol. 59:2014-2021. The genes responsible for the biosynthesis of the lantibiotics are organized in operon-like structures. The biosynthesis locus of all members in the subgroup AI lantibiotics consists of lanA, the structural gene for the lantibiotic; lanB and lanC, the modifying enzyme genes for post-translational modification of the preprolantibiotic; lanP, the protease gene for processing of the prelantibiotic; and lanT, the ABC transporter for secretion of the lantibiotic. In addition, epidermin and gallidermin have an extra gene, lanD, which is responsible for the C-terminal oxidative decarboxylation of the lantibiotic. Kupke et al. (1994) J. Biol. Chem. 269:5653-5659; Kupke et al. (1995) J. Biol. Chem. 270:11282-89. In comparison, subgroup AII lantibiotics have simpler genomic organizations. In subgroup AII, lanB and lanC are combined into one gene, lanM, and lanP and lanT are combined into lanT. Chen et al. (1999) Appl. Environ. Microbiol. 65:1356-1360; Qi et al. (1999) Appl. Environ. Microbiol. 65:652-658; Rince et al. (1994) Appl. Environ. Microbiol 60:1652-1657. All lantibiotic loci also contain a set of immunity genes, which are responsible for self-protection of the producer strains. Saris et al. (1996) Antonie van Leewenhoek 69:151-159. Moreover, the expression of the lantibiotic genes is usually regulated either by a single transcription regulator (Peschel et al. (1993) Mol. Microbiol. 9:31-39; Qi et al. (1999) Appl. Environ. Microbiol. 65:652-658) or by a two-component signal transduction system (de Ruyter et al. (1996) J. Bacteriol. 178:3434-3439; Klein et al. (1993) Appl. Environ. Microbiol. 59:296-303; Kuipers et al. (1995) J. Biol. Chem. 270:27295-27304).

[0006] Previously, the isolation, biochemical and genetic characterizations of mutacin II, produced by a group II strain of the oral bacteria Streptococcus mutans was reported. Chen et al. (1999) Appl. Environ. Microbiol 65:1356-1360; Novak et al. (1994) J. Bacteriol. 176:4316-4320; Novak et al. (1996) Anal Biochem. 236:358-360; Qi et al. (1999) Appl. Environ. Microbiol. 65:652-658. Mutacin II belongs to subgroup AII in the lantibiotic family. Recently, the isolation and genetic characterization of mutacin III from the group III S. mutans strain UA787 was reported. Qi et al. (1999) Appl. Environ. Microbiol. 65:3880-3887. The mature mutacin III is twenty-two amino acids in size, and shows striking similarity with another lantibiotic, epidermin, produced by Staphylococcus epidermidis. Allgaier et al. (1986) Eur. J. Biochem. 160:9-22. The mutacin III biosynthesis gene locus consists of eight genes in the order of mutR, -A, -A′, -B, -C, -D, -P, and T. The genomic organization and primary sequence of mutacin III places it in subgroup AI with epidermin and gallidemin as its closest neighbors. Applicants disclosed herein the biochemical and genetic characterization of mutacin I. Comparison of the biosynthesis genes between mutacin I and mutacin III reveal striking similarities as well as important differences.

[0007] The cloning and sequencing of the novel mutacin I biosynthetic genes by using information from the conserved sequence derived from several other lantibiotics, and the isolation and purification of mutacin I is disclosed herein and provides a novel group of antibiotics which can be utilized as anti-microbial agents against, for example, presently antibiotic resistant microorganisms.

SUMMARY OF THE INVENTION

[0008] According to the present invention, an isolated and purified DNA sequence which encodes a lantibiotic, mutacin I, is disclosed. The nucleic acid sequence is set forth in SEQ ID No: 1 and the amino acid sequence is set forth in SEQ ID No: 2. Also disclosed are pharmaceutical compositions containing mutacin I and methods for their use.

BRIEF DESCRIPTION OF THE DRAWINGS

[0009] So that the matter in which the above-recited features, advantages and objects of the invention, as well as others which will become clear, are attained and can be understood in detail, more particular descriptions of the invention briefly summarized above may be had by reference to certain embodiments thereof which are illustrated in the appended Figures. These Figures form a part of the specification. It is to be noted, however, that the appended FIGS. illustrate preferred embodiments of the invention and therefore are not to be considered limiting in their scope.

[0010]FIG. 1. (A) The mutacin III biosynthesis genes. The orientation of the genes and their relative sizes are shown. mutA is the structural gene for prepromutacin I, and mutA′ has no known function at present. mutB and -C encode the enzymes for dehydration and thioether bridge formation of premutacin I. mutD encodes a flavoprotein possibly responsible for oxidative decarboxylation of the C-terminal cycteine in premutacin I. mutP and -T code for the protease and ABC transporter, respectively, which are responsible for the processing and transportation of premutacin I. (B) Similarity between MutA and MutA′. The middle row shows the identical amino acids and the conserved changes (+). Arrowhead indicates the processing site in MutA. The leader peptide and the mature peptide moieties were determined based on MutA. (C) Effects of mutA and mutA′ mutations on mutacin I production. Cells from an overnight culture plate were stabbed on TH agar plate and incubated at 37° C. for twenty-four hours. The plate was heated at 80° C. for one hour to kill the producing bacteria, then an overnight culture of the indicator strain NY101 was overlaid on top of the plate. The plate was inspected after an overnight incubation at 37° C.

[0011]FIG. 2. Similarity between the mutacin I and mutacin III structural gene. The prepropeptides of mutacin I and mutacin III are compared using the sequence of preepidermin as a reference. The identical amino acids shared by all three lantibiotics are labeled with gray boxes, and the amino acids shared by any of two lantibiotics are labeled with an open box. The conserved sequence FNLD, which is shared by all lantibiotics in subgroup AI (29) is underlined. Brackets indicate the pairs of amino acid residues involved with thioether bridge formation in epidermin (1).

[0012]FIG. 3. Purification and EIMS analysis of mutacin I. (A) Elution profile of the first round purification of crude extract of mutacin I by reverse phase HPLC. One-ml fractions were collected along the course of elution and tested for antimicrobial activity (insert). (B) Elution profile of the second round purification using pooled fraction 6 from the first pass as starting material. Fractions 6 and 7 were active. (C) Electrospray ionization mass spectrometry (EIMS) of the purified mutacin I. The mass to charge ratio (m/z) for the doubly-charged molecule (1183) and the triply-charged molecule (788) are labeled. The estimated molecular weight was 2364 Da.

[0013]FIG. 4. Biochemical characterization of mutacin I. (A) EIMS analysis of the ethanethiol-derivatized mutacin I. Peaks 1 and 2 are the doubly-charged molecule of 1791 Da and 1774 Da, respectively. The 1774-Da molecule may be a deaminated form of the 1792 Da molecule. Peak 3 may be a deaminated form of peak 4, both of which are singly charged. Peak 5 and peak 6 are triply-charged and doubly-charged molecule of 2719 Da, respectively. Peak 7 is a doubly-charged molecule of 2736 Da, which gives rise to the deaminated form of 2719 Da (peaks 5 and 6). Peak 8 is a singly-charged, deaminated form of peak 9, which has a molecular mass of 1793 Da. The expected molecular mass of mutacin I after insertion of six molecules of ethanethiol is 2736 Da (2364+62×6), which correlated very well with the measured mass of 2736 as shown by peak 7. Addition of the two molecular masses of 1791 (peak 1) and 965 (peak 4) results in a molecular mass of 2756 Da, which would correlate well with the intact modified mutacin I of 2736 Da plus one molecule of H₂O (from breakage of the molecule). (B) Proposed structure of mutacin I based on the data presented in (A) and in FIG. 2. Arrowhead indicates the position where the peptide bound is broken in the ethanethiol-modified mutacin I. The calculated molecular mass for each fragment is labeled. (C) EIMS analysis of mutacin III derivatized with ethanethiol under the same conditions as for mutacin I. The expected molecular mass for fully derived mutacin III is 2636 (see Table 1), and the measured molecular mass is 2638 from the doubly and triply charged peaks (peaks 2 and 3). The 2620-Da molecule as shown by peaks 1 and 4 are probably the deaminated form of the 2638-Da molecule. The 2576-Da molecule as shown in peak 5 resulted from addition of five molecules of ethanethiol (see Table 1).

DETAILED DESCRIPTION OF THE INVENTION

[0014] The present invention provides an isolated and purified DNA sequence (SEQ ID No: 1) encoding for a novel lantibiotic, mutacin I, that has been isolated and characterized from Streptococcus mutans CH43.

[0015] Further, the present invention provides the isolated and purified DNA sequence for mutacin I designated as mutA (SEQ ID No: 1) and polymorphisms thereof specific for mutacin I.

[0016] By “isolated” it is meant separated from other nucleic acids found in bacteria. By “specific” is meant an isolated sequence which encodes the protein mutacin I.

[0017] Further, the present invention provides the amino acid sequence of the mutacin I structural protein SEQ ID No: 2, designated MutA and also referred to herein as mutacin I, functional variants thereof. The mutacin I protein has a molecular weight of approximately 2364 Da and is comprised of twenty-four amino acids in its mature form.

[0018] Modification to the nucleic acids of the present invention are also contemplated as long as the essential structure and function of the polypeptide encoded by the nucleic acids are maintained. Likewise, fragments used as primers or probes can have substitutions as long as enough complementary bases exist for selective, specific hybridization with high stringency.

[0019] Polymorphisms are variants in the gene sequence. They can be sequence shifts found between various bacterial strains and isolates which, while having a different sequence, produce functionally equivalent gene products. Polymorphisms also encompass variations which can be classified as alleles and/or mutations which can produce gene products which may have an altered function. Polymorphisms also encompass variations which can be classified as alleles and/or mutations which either produce no gene product, an inactive gene product, or increased levels of gene product.

[0020] The present invention also includes vectors including the mutacin I genes disposed therein. Such vectors are known or can be constructed by those skilled in the art and should contain all expression elements necessary to achieve the desired transcription of the sequences. Other beneficial characteristics can also be contained within the vectors such as mechanisms for recovery of the nucleic acids in a different form. Phagemids are a specific example of such beneficial vectors because they can be used either as plasmids or as bacteriophage vectors. Examples of other vectors include viruses such as bacteriophages, baculoviruses, and retroviruses, DNA viruses, cosmids, plasmids, liposomes, and other recombination vectors. The vectors can also contain elements for use in either prokaryotic or eukaryotic host systems. One of ordinary skill in the art will know which host systems are compatible with a particular vector.

[0021] The vectors can be introduced into cells or tissues by any one of a variety of known methods within the art. Such methods can be found generally described in Sambrook et al., Molecular Cloning: A Laboratory Manual, Cold Springs Harbor Laboratory, New York (1989, 1992) and Ausubel et al., Current Protocols in Molecular Biology, John Wiley and Sons, Baltimore, Md. (1989); Chang et al., Somatic Gene Therapy, CRC Press, Ann Arbor, Mich. (1995); Vega et al., Gene Targeting, CRC Press, Ann Arbor, Mich. (1995); Vectors: A Survey of Molecular Cloning Vectors and Their Uses, Butterworths, Boston, Mass. (1988); and Gilboa et al. (1986) and include, for example, stable or transient transfection, lipofection, electroporation and infection with recombinant viral vectors. Introduction of nucleic acids by infection offer several advantages over other listed methods. Higher efficiencies can be obtained due to their infectious nature. Moreover, viruses are very specialized and typically infect and propagate in specific cell types. Thus, their natural specificity can be used to target the vectors to specific cell types in vivo or within a tissue or mixed culture of cells. The viral vectors can also be modified with specific receptors or ligands to alter target specificity through receptor mediated events.

[0022] The above discussion provides a factual basis for the preparation and use of mutacin I. The methods used with and the utility of the present invention can be shown by the following non-restrictive examples and Figures.

[0023] DNA segments encoding a mutacin gene can be introduced into recombinant host cells and employed for expressing a mutacin I protein or peptide. The introduction of the mutacin I expressing DNA can be accomplished, for example, by the introduction of an organism transformed with the mutacin encoding DNA to act as a probiotic and produce the mutacin I in situ to protect against pathogens or other undesirable organisms. Alternatively, through the application of genetic engineering techniques, subportions or derivatives of selected mutacin I genes can be employed. Equally, through the application of site-directed mutagenesis techniques, one may re-engineer DNA segments of the present invention to alter the coding sequence, e.g., to introduce improvements to the antibiotic actions of the resultant protein or to test such mutants in order to examine their structure-function relationships at the molecular level. Where desired, one may also prepare fusion peptides, e.g., where the mutacin I coding regions are aligned within the same expression unit with other proteins or peptides having desired functions, such as for immunodetection purposes (e.g., enzyme label coding regions).

[0024] Pharmaceutical Compositions and Formulations

[0025] Because of the broad spectrum of activity of mutacin I against a variety of microorganisms, mutacin I can be employed to treat multiple drug resistant bacteria such as certain strains of S. aureus which are known to be multiple drug resistant.

[0026] Pharmaceutical compositions comprising the disclosed mutacins may be orally administered, for example, with an inert diluent or with an assimilable edible carrier or they may be enclosed in hard or soft shell gelatin capsules or they may be compressed into tablets or may be incorporated directly with the food of the diet.

[0027] A therapeutically effective amount is an amount of mutacin I polypeptide, the pharmaceutically acceptable salts, esters, amides, and prodrugs thereof, that when administered to a patient or subject, ameliorates a symptom of the condition or disorder.

[0028] The compounds of the present invention can be administered to a patient either alone or as part of a pharmaceutical composition.

[0029] As used herein, “pharmaceutically acceptable carrier” includes any and all solvents, dispersion media, coatings, antibacterial and antifungal agents, isotonic and absorption delaying agents and the like. The use of such media and agents for pharmaceutical active substances is well known in the art. Except insofar as any conventional media or agent is incompatible with the active ingredient, its use in the therapeutic compositions is contemplated. Supplementary active ingredients can also be incorporated into the compositions.

[0030] For oral prophylaxis, the polypeptide may be incorporated with excipients and used in the form of non-ingestible mouthwashes, dentifrices or chewing-type gums. A mouthwash may be prepared incorporating the active ingredient in the required amount in an appropriate solvent, such as a sodium borate solution (Dobell's Solution). Alternatively, the active ingredient may be incorporated into an antiseptic wash containing sodium borate, glycerin and potassium bicarbonate. The active ingredient may also be dispersed in dentifrices, including: gels, pastes, powders and slurries. The active ingredient may be added in a therapeutically effective amount to a paste dentifrice that may include water, binders, abrasives, flavoring agents, foaming agents, and humectants.

[0031] The active compounds may be orally administered, for example, with an inert diluent or with an assimilable edible carrier, or they may be enclosed in hard or soft shell gelatin capsules, or they may be compressed into tablets, or they may be incorporated directly with the food of the diet. For oral therapeutic administration, the active compounds may be incorporated with excipients and used in the form of ingestible tablets, buccal tablets, troches, capsules, elixirs, suspensions, syrups, wafers, and the like. Such compositions and preparations should contain at least 0.1% of active compound. The percentage of the compositions and preparations may, of course, be varied and may conveniently be between about 2 to about 60% of the weight of the unit. The amount of active compounds in such therapeutically useful compositions is such that a suitable dosage will be obtained.

[0032] The tablets, troches, pills, capsules and the like may also contain the following: a binder, as gum tragacanth, acacia, cornstarch, or gelatin; excipients, such as dicalcium phosphate; a disintegrating agent, such as corn starch, potato starch, alginic acid and the like; a lubricant, such as magnesium stearate; and a sweetening agent, such as sucrose, lactose or saccharin may be added or a flavoring agent, such as peppermint, oil of wintergreen, or cherry flavoring. When the dosage unit form is a capsule, it may contain, in addition to materials of the above type, a liquid carrier. Various other materials may be present as coatings or to otherwise modify the physical form of the dosage unit. For instance, tablets, pills, or capsules may be coated with shellac, sugar or both. A syrup or elixir may contain the active compounds sucrose as a sweetening agent, methyl and propylparabens as preservatives, a dye and flavoring, such as cherry or orange flavor. Of course, any material used in preparing any dosage unit form should be pharmaceutically pure and substantially non-toxic in the amounts employed. In addition, the active compounds may be incorporated into sustained-release preparation and formulations.

[0033] The active compounds may also be administered parenterally, e.g., formulated for intravenous, intramuscular, or subcutaneous injection. Solutions of the active compounds as free base or pharmacologically acceptable salts can be prepared in water suitably mixed with a surfactant, such as hydroxypropylcellulose. Dispersions can also be prepared in glycerol, liquid polyethylene glycols, and mixtures thereof and in oils. Under ordinary conditions of storage and use, these preparations contain a preservative to prevent the growth of microorganisms.

[0034] The pharmaceutical forms suitable for injectable use include sterile aqueous solutions or dispersions and sterile powders for the extemporaneous preparation of sterile injectable solutions or dispersions. In all cases the form must be sterile and must be fluid to the extent that easy syringability exists. It must be stable under the conditions of manufacture and storage and must be preserved against the contaminating action of microorganisms, such as bacteria and fungi. The carrier can be a solvent or dispersion medium containing, for example, water, ethanol, polyol (for example, glycerol, propylene glycol, and liquid polyethylene glycol, and the like), suitable mixtures thereof, and vegetable oils. The proper fluidity can be maintained, for example, by the use of a coating, such as lecithin, by the maintenance of the required particle size in the case of dispersion and by the use of surfactants. The prevention of the action of microorganisms can be brought about by various antibacterial and antifungal agents, for example, parabens, chlorobutanol, phenol, sorbic acid, thimerosal, and the like. In many cases, it will be preferable to include isotonic agents, for example, sugars or sodium chloride. Prolonged absorption of the injectable compositions can be brought about by the use in the compositions of agents delaying absorption, for example, aluminum monostearate and gelatin.

[0035] Sterile injectable solutions are prepared by incorporating the active compounds in the required amount in the appropriate solvent with various of the other ingredients enumerated above, as required, followed by filtered sterilization. Generally, dispersions are prepared by incorporating the various sterilized active ingredients into a sterile vehicle which contains the basic dispersion medium and the required other ingredients from those enumerated above. In the case of sterile powders for the preparation of sterile injectable solutions, the preferred methods of preparation are vacuum-drying and freeze-drying techniques which yield a powder of the active ingredient plus any additional desired ingredient from a previously sterile-filtered solution thereof.

[0036] Dosage forms for topical administration of a compound of this invention include ointments, powders, sprays, and inhalants. The active component is admixed under sterile conditions with a physiologically acceptable carrier and any preservatives, buffers, or propellants as may be required. Ophthalmic formulations, eye ointments, powders, and solutions are also contemplated as being within the scope of this invention.

[0037] Intravascular devices, such as catheters, have become indispensable tools in the care of seriously ill patients. It is estimated that in the United States alone, 150 million catheters are purchased each year. However, due to the morbidity and mortality resulting from catheter-related infections and the high cost of managing such complications, the benefit derived from these devices may be offset. It has been shown that bloodstream infection due to the use of intravascular catheters (IVC) increased dramatically during the last ten years. From 1975 to 1977, an estimated 3% infection occurred among IVC users, while in 1992 to 1993, this rate increased to 19%. The death rate from such infection is ˜8000 to 16000 per year, exceeding the death rate for AIDS. The cost for treating IVC-related infections is ˜132 to 1600 million per year.

[0038] Most infections came from the human skin and the hub of the catheter. Among the infectious bacteria, 40% are coagulase-negative staphylococci, such as S. epidermidis, and 14% are coagulase-positive S. aureus. The remaining are mostly other gram-positive bacteria such as bacilli and enterococci.

[0039] Prophylactic methods have been developed to prevent IVC-related infections. The first line of treatment is to sterilize the insertion site with iodine and 70% ethanol. However, compliance with the written protocol is low; only 23% operations follow the protocol. Another preventative measure is the use of catheters impregnated with antibiotics or antiseptic agents such as chlorhexidine and silver sulfadiazine. In clinical trials, mixed results were obtained using such catheters. In addition to the problem of drug resistance by the infecting bacteria, the antibiotics coating the catheters can also be washed away by body fluid, as the attachment of antibiotics to the catheter surface is mainly through ionic interactions.

[0040] Because of the urgency to solve the problem of IVC-related infection and the growing market for development of catheters resistant to bacterial attachment on the surface thereof, mutacins are an excellent choice for prevention of IVC-related infections. Mutacin I has the following advantages over conventional antimicrobial agents: 1) it has a wide spectrum of antimicrobial activity against a wide range of gram-positive bacteria including the multidrug-resistant Staphylococci and Enterococci, the major culprits of IVC-related infections; 2) due to its unique mode of action against the sensitive bacteria, resistance to mutacin has not been observed; 3) mutacin is highly thermostable and works in a wide range of pH which makes it suitable for use in a wide range of conditions; 4) its hydrophobic nature can be advantageous for coating the surface of catheters and preventing adhesion of bacteria to the surface; and 5) because it is produced by a normal member of the human oral biota, it is unlikely to elicit immune response from the patient or has any toxicity to the host.

[0041] Active mutacin I compound can be coated onto intravascular devices and/or linked to polymers used in the manufacture of these devices to be used to prevent infection caused by intravascular devices. The mutacin I compounds of the present invention can be utilized alone in combination with at least one other entity, such as linked to a polymer, for the prevention or reduction of infection associated with a variety of medical devices such as indwelling tubes or catheters, artificial valves, pacemakers, implantable devices, etc., by incorporating, coating, or otherwise combining the active mutacin I compounds with the materials comprising the patient contact portions of the medical devices. The polymer can be a hydrophobic material or matrix that can be attached to an indwelling device such as a catheter through hydrophobic bonding or can be tethered to the indwelling device through a molecular linker. The incorporation and/or combination of the active mutacin I compounds may be accomplished by coating the medical devices with active mutacin I compounds or by incorporating the active mutacin I compounds into the structure of the medical device. Because the mutacin I compounds of the present invention are very heat stable, they are able to withstand the conditions associated with their incorporation into the medical devices. By combining and/or incorporating the active mutacin I compounds of the present invention into medical devices, both active and passive infection control can be achieved at sites or for uses, which, in many instances, are highly susceptible or vulnerable to infection.

[0042] The term “pharmaceutically acceptable salts, esters, amides, and prodrugs” as used herein refers to those carboxylate salts, amino acid addition salts, esters, amides, and prodrugs of the compounds of the present invention which are, within the scope of sound medical judgment, suitable for use in contact with the tissues of patients without undue toxicity, irritation, allergic response, and the like, commensurate with a reasonable benefit/risk ratio, and effective for their intended use, as well as the zwitterionic forms, where possible, of the compounds of the invention. The term “salts” refers to the relatively non-toxic, inorganic and organic acid addition salts of compounds of the present invention. These salts can be prepared in situ during the final isolation and purification of the compounds or by separately reacting the purified compound in its free base form with a suitable organic or inorganic acid and isolating the salt thus formed. Representative salts include the hydrobromide, hydrochloride, sulfate, bisulfate, nitrate, acetate, oxalate, valerate, oleate, palmitate, stearate, laurate, borate, benzoate, lactate, phosphate, tosylate, citrate, maleate, fumarate, succinate, tartrate, naphthylate mesylate, glucoheptonate, lactobionate and laurylsulphonate salts, and the like. These may include cations based on the alkali and alkaline earth metals, such as sodium, lithium, potassium, calcium, magnesium, and the like, as well as non-toxic ammonium, quaternary ammonium and amine cations including, but not limited to ammonium, tetramethylammonium, tetraethylammonium, methylamine, dimethylamine, trimethylamine, triethylamine, ethylamine, and the like. (See, for example, Barge et al., “Pharmaceutical Salts,” J. Pharm. Sci., 1977, 66:1-19 which is incorporated herein by reference.)

[0043] Examples of pharmaceutically acceptable, non-toxic esters of the compounds of this invention include C₁-C₆ alkyl esters wherein the alkyl group is a straight or branched chain. Acceptable esters also include C₅-C₇ cycloalkyl esters as well as arylalkyl esters such as, but not limited to benzyl. C₁-C₄ alkyl esters are preferred. Esters of the compounds of the present invention may be prepared according to conventional methods.

[0044] Examples of pharmaceutically acceptable, non-toxic amides of the compounds of this invention include amides derived from ammonia, primary C₁-C₆ alkyl amines and secondary C₁-C₆ dialkyl amines wherein the alkyl groups are straight or branched chain. In the case of secondary amines, the amine may also be in the form of a 5- or 6-membered heterocycle containing one nitrogen atom. Amides derived from ammonia, C₁-C₃ alkyl primary amines, and C₁-C₂ dialkyl secondary amines are preferred. Amides of the compounds of the invention may be prepared according to conventional methods.

[0045] The term “prodrug” refers to compounds that are rapidly transformed in vivo to yield the parent compounds of the above formula, for example, by hydrolysis in blood. A thorough discussion is provided in T. Higuchi and V. Stella, “Pro-drugs as Novel Delivery Systems,” Vol. 14 of the A.C.S. Symposium Series, and in Bioreversible Carriers in Drug Design, ed. Edward B. Roche, American Pharmaceutical Association and Pergamon Press, 1987, both of which are incorporated herein by reference.

[0046] In addition, the compounds of the present invention can exist in unsolvated as well as solvated forms with pharmaceutically acceptable solvents such as water, ethanol, and the like. In general, the solvated forms are considered equivalent to the unsolvated forms for the purposes of the present invention.

[0047] The compounds of the present invention can be administered to a patient at various dosage. For example, the dosage can depend on a number of factors including the requirements of the patient, the severity of the condition being treated, and the pharmacological activity of the compound being used. The determination of optimum dosages for a particular patient is well known to those skilled in the art.

EXAMPLES

[0048] Materials and Methods

[0049] Bacterial Strains and Media.

[0050] The group I S. mutans strain CH43 originated from a Chinese school child as part of a natural history study of human caries. Strain CH43 contains a cryptic plasmid similar to other 5.6-kb plasmids within the S. mutans Group I strains. S. sanguis strain NY101 was used as the indicator for mutacin activity assays. CH43 and NY101 were grown on Todd-Hewitt (TH) plate with 1.6% agar (Difco Laboratories, Detroit, Mich.) unless indicated otherwise.

[0051] Cloning and Sequencing of the Mutacin I Biosynthetic Genes.

[0052] Cloning and sequencing of the mutacin I biosynthesis genes were performed exactly as described previously. Qi et al. (1999) Appl. Environ. Microbiol. 65: in press.

[0053] Insertional Inactivation.

[0054] The mutA and mut′ genes were inactivated separately by insertion of a kanamycin-resistant gene cassette exactly as described for mutacin III. Qi et al. (1999) Appl. Environ. Microbiol. 65:625-658.

[0055] Isolation and Purification of Mutacin I.

[0056] For mutacin production, CH43 was grown on TH/agar plate for one day under anaerobic conditions. The cells were then spread on a PHWP membrane with 0.3 μm pore size (Millipore Corp., Bedford, Mass.) on top of a TH plate containing 0.3% agarose. The plate was incubated at 37° C. for two days anaerobically. The membrane was transferred to a new plate for continued incubation every two days, and the old plate was frozen at −70° C. For mutacin isolation, the plates were thawed quickly in a 60° C. water bath. The liquid medium was separated from the agarose debris by centrifugation and the supernatant was passed through a membrane with 0.45 μm pore size. Mutacin I was extracted with an equal volume of chloroform. Novak et al. (1994) J. Bacteriol. 176:4316-4320. The precipitate was dried under a stream of air and washed once with double-distilled H₂O (ddH₂O). The water-insoluble material (crude extract) was dissolved in 6 M urea and tested for antimicrobial activity by a plate assay after a serial dilution with ddH₂O. One arbitrary unit of activity (AU) was defined as the highest dilution that showed a clear zone of inhibition of the indicator strain NY101.

[0057] For purification, the crude extract of mutacin I was applied to a Source 15RPC column and eluted with a fragmented gradient A (0.1% TFA) and B (0.085% TFA in 60% acetonitrile) using a LKB Purifier (Amersham Pharmacia Biotech, Piscataway, N.J.). The active fractions were pooled and dried in a lyophilizer. The pellet was redissolved in 0.25% TFA and subjected to a second round purification using a fragmented gradient of buffer A (0.1% TFA) and B (0.085% TFA in 80% methanol). The single active peak fraction was collected, dried in a lyophilizer, and used for sequence analysis and electrospray ionization mass spectrometry (EIMS).

[0058] Chemical Modification of Mutacin I.

[0059] Fifty micrograms of purified mutacin I were dried under vacuum and resuspended in 90 μl of a derivatization mixture consisting of 280 μl ethanol, 200 μl water, 65 μl 5M sodium hydroxide, and 60 μl ethanethiol as described). Meyer et al. (1994) Anal. Biochem. 223:185-190. The reaction proceeded at 50° C. for one hour under nitrogen, then stopped by the addition of 2 μl acetic acid. The reaction mixture was dried under vacuum and washed three times with 50% ethanol. The pellet was resuspended in 10 μl of 50% acetonitrile with 1% formic acid for EIMS analysis and peptide sequencing by Edman degradation.

[0060] Nucleic Acid Accession Numbers:

[0061] The sequence for the mutacin I operon has been submitted to Genbank with the accession #AF207710 (AF267498), also designated SEQ ID No: 3.

Results

[0062] Cloning and Sequencing of the Mutacin I Biosynthetic Genes.

[0063] As described previously (Qi et al. (1999) Appl Environ. Microbiol. 65:652-658), while isolating mutacin III biosynthesis genes by PCR amplification using a pair of primers designed based on the conserved sequences among LanA and LanB proteins, the mutacin I biosynthesis genes were isolated using the same primers. Sequencing of the isolated PCR fragment demonstrated a striking similarity between the mutacin I and mutacin III genes. By chromosomal walking, the major part of the mutacin I biosynthesis operon was cloned and sequenced as shown in FIG. 1A. It consists of eight genes in the order of mutR, -A, -A′, -B, -C, -D, -P, and -T, which is possibly followed by the immunity gene mutF (SEQ ID No: 12). As in the mutacin III operon, MutR (SEQ ID No: 4) was the positive regulator for the expression of the mutacin I operon (Qi et al. (1999) Appl. Environ. Microbiol. 65:652-658. MutA (SEQ ID No: 5) and MutA′ (SEQ ID No: 6) showed strong similarity to each other as shown in FIG. 1B. Insertional inactivation of mutA and mutA′ demonstrated that mutA was required for mutacin I production, while mutA′ was not as shown in FIG. 1C. This result suggested that, like mutA in the mutacin III operon, the mutA in the mutacin I operon was likely the structural gene encoding prepromutacin I. MutB (SEQ ID No: 7), -C (SEQ ID No: 8) and -D (SEQ ID No: 10) possibly constituted the modification apparatus for prepromutacin I, and MutT (SEQ ID No: 11) and -P (SEQ ID No: 10) are the ABC transporter and protease for transportation and processing of premutacin I, respectively. Other gene encoded mutacin I peptides include MutF (SEQ ID No: 12), MutE (SEQ ID No: 13), MutG (SEQ ID No: 14), OrfX (SEQ ID No: 15), OrfY (SEQ ID No: 16), and OrfZ (SEQ ID No: 17).

[0064] Similarity between Mutacin I and Mutacin III Biosynthesis Genes.

[0065] The overall similarity between mutacin I and mutacin III biosynthesis genes was ˜94% at the nucleotide level over the 10 kb operon. However, the differences between the two operons were not distributed evenly among the different genes. For example, from mutR to the region immediately upstream of mutA, the similarity was 99%, while in the mutA and mutA′ coding regions, the similarity was only 89% and 91%, respectively. At the amino acid level, the two MutAs shared 84% identical residues as shown in FIG. 2, and the two MutA's shared 93% identical residues. For MutB and MutC the similarity was 93% and 95%, respectively. An even higher similarity (99%) existed in MutP and -T between the two strains.

[0066] Purification of Mutacin I.

[0067] To biochemically characterize mutacin I, sufficient amount of starting material is required. Applicants' first attempt to isolate mutacin I from liquid culture failed because no mutacin I was produced in any of the liquid cultures that were tested. A stab culture on TH/agarose plate as described for mutacin III was then tried. Qi et al. (1999) Appl. Environ. Microbiol. 65:652-658. Mutacin I was produced on such a plate, however the production level was still too low for satisfactory isolation. Based on the observation that mutacin I could be produced on all solid media plates regardless of the media composition, it was reasoned that the production of mutacin I may be regulated by a cell-density mediated control mechanism similar to quorum sensing. (Kleerebezem et al. (1997) Mol. Microbiol. 24:895-904; Surette et al. (1999) Proc. Natl. Acad. Sci. USA 96:1639-1644). Based on this rationale, a membrane transfer technique as described in Materials and Methods was employed, which resulted in a high level of mutacin I production.

[0068] Mutacin I was purified by reverse-phase HPLC as shown in FIG. 3. The active fraction (fraction 6) from the first pass (see FIG. 3A) was collected and subjected to a second round purification using a different buffer B and a different gradient (see FIG. 3B). The active fractions (fractions 6 and 7) from the second pass were dried under vacuum and tested for purity by EIMS analysis. As shown in FIG. 3C, mutacin I was purified to near homogeneity as judged by the lack of significant background peaks in the MS chromatogram.

[0069] Characterization of Mutacin I by Ethanethiol Derivatization and MS Analyses.

[0070] The molecular weight of mutacin I was measured by electrospray ionization mass spectrometry. The mass-to-charge ratio for the doubly-charged molecule was 1183, and that for the triply-charged molecule was 788 as shown in FIG. 3C. Thus the measured molecule mass was 2364 Da. This value was in a good agreement with the calculated value of 2516 Da for the unmodified mutacin I minus six molecules of water (108 Da) and one molecule of carboxy residue (45 Da from decarboxylation at the C-terminal cycteine residue).

[0071] The primary sequence of mutacin I contained six serine residues and one threonine residue, all of which were potential sites for post-translational dehydration. To confirm that there were indeed six dehydrated residues in the mature mutacin I, an ethanethiol modification of mutacin I under alkaline conditions was performed. In this reaction, one molecule of ethanethiol could insert into the thioether bridge, resulting in a S-ethylcystein and a cystein, or it could insert into the double bound of a dehydrated serine or threonine to form a S-ethylcystein or a β-methyl-S-ethylcycteine. Meyer et al. (1994) Anal. Biochem. 223:185-190; Novak et al. (1996) Anal. Biochem. 236:358-360. Ethanethiol derivatization of lantibiotics has been used prior to sequencing of the other lantibiotic gallidemin and pep5 (Meyer et al. (1994) Anal. Biochem. 223:185-190), and for determination of the number of dehydrated amino acid residues in mutacin II (Novak et al. (1996) Anal. Biochem. 236:358-360). The expected molecular mass of mutacin I after each addition of an ethanethiol molecule is listed in Table 1. TABLE 1 Expected molecular masses of ethanethiol derivatives of mutacins I and III Expected mass (Da) Mutacin 0* 1 2 3 4 5 6 I 2,364 2,426 2,487 2,549 2,611 2,673 2,738 III 2,264 2,318 2,390 2,452 2,514 2,576 2,638

[0072] Quite surprisingly, none of the major peaks generated after ethanethiol modification of mutacin I had the expected molecular mass as shown in FIG. 4A. A very small portion of the molecules showed a pass of 2736 Da (Peak 7), which could account for mutacin I plus six molecules of ethanethiol (2364+62×6); the result of the molecules were all much smaller than expected. With close inspection and calculations, the identity of the small molecules was determined. As shown in FIG. 4B, it appeared that the majority of mutacin I molecules broke into two fragments after the addition of six molecules of ethanethiol. The larger fragment with a mass of 1791 Da was the N-terminal part from F-1 to N-16, and the smaller fragment (965 Da) was the C-terminal part from P-17 to C-24. This finding was of interest because the closely related mutacin III molecule remained intact after the same modification reaction under the same conditions as shown in FIG. 4C.

[0073] Peptide Sequencing of Unmodified and Ethanethiol Modified Mutacin I.

[0074] Comparison of mutacin I and mutacin III revealed that mutacin I had seven potential dehydration sites (six serines and one threonine), while mutacin III had six (four serines and two threonines). Interestingly, both mutacins had six ethanethiol additions after ethanethiol modification (see FIGS. 4A and 4C), suggesting that all serine or threonine residues in mutacin III were dehydrated. To determine which serine or threonine residue was not dehydrated in mutacin I, the purified mutacin I was subjected to peptide sequencing by Edman degradation. With native mutacin I, Edman degradation was blocked after the first F residue, suggesting that the second serine residue is dehydrated. Dehydrated amino acids were shown to block Edman degradation in other lantibiotics. Gross et al. (1971) J. Am. Chem. Soc. 93:4634-4635; Mota-Meira et al. (1997) FEBS Lett. 410:275-279; Novak et al. (1994) J. Bacteriol. 176:4316-4320.

[0075] To get a complete sequence of mutacin I, the ethanethiol-derivatized mutacin I had to be used. Ethanethiol-derivatization of lantibiotics was shown to allow Edman degradation to proceed through the dehydrated serine and threonine residues and thioether bridges in other lantibiotics. Meyer et al. (1994) Anal. Biochem. 223:185-190; Mota-Meira et al. (1997) FEBS Lett. 410:275-279. Since the majority of mutacin I molecules was broken into two fragments (see FIG. 4) during ethanethiol modification, the C-terminal fragment had to be eliminated to solve the problem of having two N-termini in the reaction mixture. After several trials, the C-terminal fragment was eliminated by washing the reaction mixture with 30% acetonitrile. The pellet fraction after 30% acetonitrile wash contained mostly the full-length modified mutacin I and the N-terminal fragment. Sequencing of the pellet fraction revealed the following sequence: F₁-SEC₂-SEC₃-L₄-SEC₅-L₆-SEC₇-SEC₈-L₉-G₁₀-SEC₁₁-T₁₂-G₁₃-V₁₄-K₁₅-N₁₆-P₁₇-SEC₁₈-F₁₉-N₂₀-SEC₂₁-Y₂₂-SEC₂₃. S-ethylcysteine (SEC) was the product of ethanethiol insertion into the double bond of dehydrated serine, or the thioether bridge in lanthionine. The results revealed that all six serine residues in the mutacin I molecule were dehydrated, and that T-12 remained as a nondehydrated residue. In addition, a closer look at the HPLC chromatogram of the sequencing reaction of mutacin I revealed minor peaks in the sequence of P-x-F-N-x-Y. This sequence correlated with the C-terminal fragment of mutacin I: P₁₇-S₁₈-F₁₉-N₂₀-S₂₁-Y₂₂-C₂₃-C₂₄. This result corroborated the previous assignment for the two peptide fragments generated during ethanethiol modification as shown in FIG. 4B.

[0076] The mutacin I biosynthesis genes from the group I strain of S. mutans CH43 were cloned and sequenced. DNA and protein sequence analysis revealed that mutacin I and mutacin III are highly homologous to each other, likely arising from a common gene ancestor. Mutacin I was produced by a membrane transfer technique and purified to homogeneity by reverse phase HPLC. The mature mutacin I is twenty-four amino acids in size with a molecular weight of 2364 Da. Ethanethiol modification of mutacin I revealed that it contains six dehydrated amino acids. Sequencing of the native and ethanethiol-derivatized mutacin I by Edman degradation demonstrated that mutacin I is encoded by mutA, and that the six serine residues in the primary sequence of mutacin I are dehydrated, four of which are possibly involved with thioether bridge formation. Comparison of the primary sequence of mutacin I with that of mutacin III and epidermin suggests that mutacin I likely possesses the same bridging pattern as epidermin.

[0077] A closer inspection of the differences between the homologous genes of mutacin I and mutacin III revealed that they are not all distributed evenly. For MutR, -D, -P, and -T, the homology is over 99% between the two mutacins, while for MutA, -A′, -B, and -C, the similarity varies from 87 to 95%. The distribution of the variations within a protein is not even either. For example, in MutA, the leader peptide region was identical between the two mutacins. However, the mature peptide region differed by 37.5% (FIG. 2). More interestingly, the sequence of the mature mutacin III is closer to that of epidermin (77% similarity) than to mutacin I (62.5% similarity), while the sequence of the leader peptide of mutacin III and epidermin are dramatically different as seen in FIG. 2. For MutB, -C, -D, -P, and -T proteins, mutacin I and mutacin III are closer to each other than to epidermin.

[0078] The biosynthesis of lantibiotics involves several posttranslational modification steps. Chakicherla et al. (1995) J. Biol. Chem. 270:23533-23539; de Vos et al. (1995) Molecular Microbiol. 17:427-437; Sahl et al. (1998) Annu. Rev. Microbiol. 52:41-79. The first step is the translation of the structural gene message into a prepropeptide. The prepropeptide is then modified by dehydration of serine and threonine residues, and formation of thioether bridges between cysteine and the dehydrated amino acid residues. The prepeptide is then translocated across the cell membrane, where the leader peptide is cleaved off and the mature peptide released to the outside medium.

[0079] One advantage of lantibiotics over classical antibiotics is its gene-encoded nature, which means that lantibiotics can be altered with ease by manipulating the structural genes through mutagenesis. In reality, however, the number of mutations that can be made is limited because the production of active lantibiotics depends on correct post-translational modification and processing.

[0080] Mutacin I and mutacin III are closely related to each other at both the nucleotide and amino acid levels. Comparison of the mature peptide sequence of mutacin I and mutacin III suggests that they may also have the same pattern of thioether bridge formation. Despite all the similarities, some important differences exist between the two mutacins. For example, ethanethiol modification of mutacin I broke the molecule into two fragments between N-16 and P-17 as shown in FIG. 4B, while the same reaction did not affect the integrity of mutacin III as shown in FIG. 4C. Comparison of the two mutacins revealed that the major difference is at the linker region (T-12 to P-17), where mutacin I has the sequence T-G-V-K-N-P, and mutacin III has the sequence A-R-T-G as shown in FIG. 2A. These different amino acid residues, according to the statistical figures of Creighton (Creighton, p. 235, in (ed.) Proteins: Structures and molecular principles, W. H. Freeman and Company, New York), have different tendencies in forming different secondary structures in proteins. For example, N-16 and P-17 in mutacin I are more likely to be involved in forming β-tums, while A-12 in mutacin III is more likely to participate in α-helix formation (Stryer, p. 37, in (ed.) Biochemistry, W. H. Freeman and Company, Biochemistry, New York). More importantly, N-16 and P-17 are absent in mutacin III.

[0081] In accordance with the possible difference in secondary and tertiary structures, mutacin I and mutacin III have different hydrophobicity and antimicrobial activity. In reverse-phase HPLC analysis, mutacin I is eluted at a higher acetonitrile concentration than mutacin III, suggesting that it is more hydrophobic than mutacin III. In antimicrobial spectrum assays with a limited set of pathogens, mutacin III is more potent than mutacin I against Staphylococcus aureus and Staphylococcus epidermidis, while both mutacins have equal activities against other pathogens such as enterococci, pneumococci, and Group A streptococci.

[0082] Any patents or publications mentioned in this specification are indicative of the levels of those skilled in the art to which the invention pertains. These patents and publications are herein incorporated by reference to the same extent as if each individual publication was specifically and individually indicated to be incorporated by reference.

[0083] One skilled in the art will readily appreciate that the present invention is well adapted to carry out the objects and obtain the ends and advantages mentioned, as well as those inherent therein. The present methods, procedures, treatments, molecules, and specific compounds described herein are presently representative of preferred embodiments, are exemplary, and are not intended as limitations on the scope of the invention. Changes therein and other uses will occur to those skilled in the art which are encompassed within the spirit of the invention as defined by the scope of the claims.

1 17 1 168 DNA Streptococcus mutans 1 atgtcaaaca cacaattatt agaagtcctt ggtactgaaa cttttgatgt tcaagaagat 60 ccaacagata ctactattgt ggcaagcaac gacgatccag atactcgttt ctcaagtttg 120 agtttaacag gggtgaaaaa tcctagtttc aatagttact gttgctaa 168 2 24 PRT Streptococcus mutans 2 Phe Ser Ser Leu Ser Leu Cys Ser Leu Gly Cys Thr Gly Val Lys Asn 1 5 10 15 Pro Ser Phe Asn Ser Tyr Cys Cys 20 3 15567 DNA Streptococcus mutans 3 aaatttgttt tttatactaa aagcgggaat gattcaaaac taaaaaagat aaacgaagaa 60 ttgaaaaagt gatataatag cacagaagag ggcctttata atgaaaggag actattttga 120 aagtaaatca atcaatggaa ttaggtgaac tttatcgaga attaagaatt gctagaggtt 180 tgaagataaa agatatagct tgtaaaaatc tgtccaagtc acaactctct agatttgaaa 240 atggacaaac catgttggca gctgataaat tgctattagc tatttcggga attcatatga 300 gtttttcgga atttggatat gctttgagcc attatgagga gagtgatttt ttcaaaaggg 360 gtaataagtt atcagaatta tatgtccaga aagatatcaa aggattaaaa aagttattag 420 aatttaatga caatcatgag gtatttgatg tctacaatcg tttaaataaa ttggttattc 480 aagttactat tcatttgcta gatactgatt acataatatc agatgatgat aagaattttt 540 taacaactta tctatataat attgaagagt ggactgagta tgaactttat atctttggaa 600 atactatgtc tatattgtca tctgatgatt taattttttt gggaaaagct tttgtagaac 660 gtgataagtt gtatatatct cttcctagtc ataagaaaaa tgcagagtta acttttttaa 720 atttaatctt aattttgctt gaaagaaaaa aattatatca agcaatctat tttgtagaga 780 atttagagaa attattaaat taccaagata tgtttgcaat aacattttta aaatttttaa 840 aaaaaattat tacttacttt catgataagt cagtagatat gtctgaatta gaacattata 900 ttaatatagt tgaagaaata aatcctacga ttgcttcaat tcttaaatct aatttgaatc 960 agcttttatc aagttttagc cattaaagcc atcttgataa attttatatc tttcatattc 1020 attaaatgtg gagataatga aaaagcaacg gttatgctat cgctgctttt tttgtgatta 1080 gaagctatgt tatcatggag ttatagtaat gaaacatagt gacagttcat catttcttat 1140 tataaaagtg gtaataagag aagtggtaaa caaagagtta gtaaaataat acgtttaacc 1200 ataatatttc ctcctttaat ttattataag attcaaaaag gtaatattcc tatatttgca 1260 aatatgggat aaaataattt taaaaaagca gatttgcaat tttaaaaaaa atagaggcta 1320 atggtggtat tatattattg taaatatatg tttactcagt aatagtgatt tactattaca 1380 acagattttg ttgttatctt agatatttct gctagcatta gttatctgta gatgtactac 1440 ttaataagta tataattata attatataat aactattatc agattaccgt taaaagtttt 1500 ctgatatgct tctactgaac aatttacgtt cagttacaca catgaaaaag gaggatatta 1560 tgtcaaacac acaattatta gaagtccttg gtactgaaac ttttgatgtt caagaagatc 1620 tctttgcttt tgatacaaca gatactacta ttgtggcaag caacgacgat ccagatactc 1680 gtttctcaag tttgagttta tgttcattag gatgtacagg ggtgaaaaat cctagtttca 1740 atagttactg ttgctaagtt gtacaaaaga tttagattgt gtcgcatgtc agcggcacaa 1800 tcttttgata ttagagatat taaatatgtt aaacacacaa ttattagaag tccttggtac 1860 taaaactttt gatgttcaag aagatttatt tgagtttaat ataacagata ctattgtact 1920 gcaggttagt gatagtccag gtactcatag taaagtgggt agtttcagta tctgtcctcc 1980 tcgaaagacc tccgtcagtt tcaatagtta ctgttgttaa ctataaatta tacttaaatt 2040 gataggaaac ttggtcatga cattatcata tgttgatatt ggaagagaat caaatttata 2100 aagacaatta aatctaaatt tgatgaatat ttagatgaat tattactagg ttgacagtca 2160 tgttaggaga agagatgaac gattttcaat ttcaagatta ttttatgtac agaaaaccat 2220 taggcaactt ttctaatttt cttagtataa ctgatatgat ggatcctatt gaattattac 2280 ataatgatcc gatatttgct gaaggggtat atttggcttc cccatctctt agatcatcta 2340 taaataaatt agagaatcag attgcaagta ctaaggaaaa aaagaatgca aaagagacta 2400 tttttcaata ctatgcccgt tataacacga gatcaactcc gtttggcttg ttttcgtcca 2460 tcggaatagg tggtttttcg aaccacccta ggaaagagaa atcttgttat gaaaaatctg 2520 ttaatgttga tcttttttgg gcttataaag tagcagataa actagaaagt atgcctgaaa 2580 ttttaaatac tttaaaagta gttgctaata atgctttgca aaagtcaaat gatttttggc 2640 ttttagatac acgaagtcat tttggactta tgaattcacg ttcagatatt cgtgaggaca 2700 ttacagttaa gtctaatcag cttatagatt atgttattaa ttgcacagaa gaaccaatta 2760 gctatcaaac attaattgat gatattgccg agaaattctc tcaatctagt gatgatgtaa 2820 aagaatattt gcaaacatta attaaagagg agtttttaat aactgaattg aaatttagtt 2880 tgattgatga taatcctttg gattggttta ttaatatttt agaaagagat caaaataact 2940 cagaattact tgaaaagttg actgaaataa aggcaatgat tcaagattat actgaccgta 3000 acataggtga aggtaacaat tcgattttag ctctagaaaa taagatgagc caaatagtaa 3060 aagccaacgc atacctgcga gttgatcttt atgatcatgc agagctgaag ttagcgcaac 3120 ataccaagag ttctcttcag aatattttga aagtactaag ttctttttcg tcagctgtta 3180 atagtcaaaa agaaattaaa aattatcatg agaaatttat tgccaggtat ggatacgagc 3240 agttagtacc tcttcaatta cttttgaatt ctactagtgg acttggtttt ccaaaagggt 3300 atagtcaaac agaagtttct aaacaaaata atgaagatag taaaaatcaa aaaataatag 3360 aatttttaca gagaaaattt gaaaaagctt taagagatgg taaagaaatt attttgagtg 3420 atgatgattt aaaagattta aattttgaca cggaacagca aatatcagga gaattatatt 3480 gtttctacaa ttttaaaagt aaaaagctag aggttagtag tttaggtgtc tcacagatgc 3540 ttggaaatac ttttggacgt ttccattcta aattgccgaa tacgatagtc acaaaaaatg 3600 taaataagac gaaagaaatt tttactgagg cttatccaaa tactattatt actcaattaa 3660 atgaagtgcc atattttggg agaggtggca atattatgat tagtaatagc cttaaaagtc 3720 accagttgga attgaggaac tatactacta aaaaagagat gagtatcaat gatatttatg 3780 tacgtgcaac cagtgaggag ttatattttt attctaagaa atatgagaaa agagttattt 3840 ttgtgatgaa taatatgttt aattatataa atggttctaa actcttacgt tttttactag 3900 aagtttcaaa ttctgatttt caaaatatta ccccgattac gcttggtagt ctggattctt 3960 ataatcatgt gcccgctatc atttataaag atattattat taaaccggaa acatggaaca 4020 ttagaaaatc tgaagctaag actttagatt ctctcaaaaa ttggctaact aataataatg 4080 ttccgccttt tgtacggatg aaatatactg atcaaattat ttatttagat ttgagtcgga 4140 ctattgattt aactatgcta tttcagagta tcaaaaaaca tagcttcata caattattag 4200 atgttcattc agtatgtaca aacgatacgg agattttaga attagttgtt ccttttacaa 4260 gaagtgatgt taacgctcac cagatttatc attatgctca gaatatttat actttggagg 4320 attcaggtag taaagaaaaa tatttttacg ctaaaattta tgtgaataaa caacgacaga 4380 cctctttcct acaaaaagag tatcctttat tattaaaata tttgaaactc ccagaaaact 4440 tacaatggtt ctatattaga tataaagatg atggaaaaga cagcatacgt ctcagaatca 4500 gatatgtaga agataaacaa ttagttcaac tttattcacg ctttatagag tgggcaacaa 4560 aagcacggaa aaatatccaa atttcaggtt atgaaattag tgaatatatc cctgaatcag 4620 caagatatgg agggaaaaaa tattcttcaa ttattcattc ttttttctat tatgatagta 4680 ttttggattt gcttttacag aagaaagcag aacaaactat tgaagtaaga acatctctca 4740 gtattattcg tatgttttta atgatgaaat taagcttaca agaccagcag aaactcataa 4800 agaatttatt tgatggaaaa cataaactta aatatgaaaa agaatatcat aattcaataa 4860 gtttattact tgacaattta tgtacaaaaa atcagacaga tgaagctgat attttctgtg 4920 taatgaatat gaaaaaaatc actgaaaaaa ttagctcagt tcttaaacaa aaggacttaa 4980 caacagattg gcagagaatt ctaggaagtt taattcatat gcgatgtaat cgagtatatg 5040 gaattaacag tgagttagaa agaaaaacaa tgtttattgt tgacaaagtt attaattcaa 5100 aaagatatac ggatatgttt ttggaggtgg gtaatgagac aaagtaaacg tgtcgaaaaa 5160 attaaagata ttctaactga gcaaacttat ttattcgatt atcaagaaat attaaaaaaa 5220 gtcagtcaag caaaacaaac agatttttgg aatttacttt ccttatcttc gggaataact 5280 tctttattaa tattttatca agagtatgag aatttagaag gagtaaactt aaagcagcaa 5340 aagcagtcat taattgggct tataagtcat tatattaatc aaatagcaga gaaatcctct 5400 ttatttgatg gtttagctgg ggtaggtttt gctattaatt atatctctaa taacggtaaa 5460 tattatcaaa aacttcttga acagattgac aacagactcc gtcagaatat tgaacggaac 5520 cttgtcaact ataagaatga ggaatatgca aatcctatga attatgatgt agtttctgga 5580 aatgctggag tagctcgcta cttgatggaa agagaatcct ctgaagattg gcgaatagtt 5640 gaaatgattt tagaaacatt ttataaagct ttagagcaag gctggcgagt acagtcaaaa 5700 tatcaatttc tagagtctga aaagcagtat tatctagaag gaaatataaa tttcgggttg 5760 gctcatggaa tattaggacc tgcgacaatt atggctcttt atcaacgaag agaaccacaa 5820 aatacaagaa atgctgagaa gcttcaagaa acttatcgac taataaaaag atacgcccag 5880 gtaagagatg aagggttacg atggccaata cgatatgatt tgtttcgtaa agagggttct 5940 tttatattac gaaatggttg gtgttatggc gagaatggca tttataatac actttttctt 6000 atgggaaaag tactctcaaa tcaggagatt tgtgaaactg ctcagaaagt tataccatcc 6060 atcataaaag atgattatga gaaaatggaa agtccaacat tttgtcacgg gtttgctgga 6120 aaagcaaatt tctttcttct gcaatatcaa agaactaaag aatcaatatt tttagttaaa 6180 gcagaagaag aaattgataa aatattaatt gtgtacaatt ctgaaaatat gtttggattt 6240 aaagatatag aagataatat tgataatact ggagagagat taacttattg ggataatttt 6300 ggtcttctta gtggaactgt tggtgttcta ttagttttga tggaatattg taatattgta 6360 aatgccggaa aaattgcaga gtggaataaa atttttcttt tgacttaatt aactgaacgg 6420 agaaataatt atggaagaac aaaatataga gaaaaaaatt ctcttgtgcc taacaggttc 6480 tggagcattg ttagggatag ctgaatatat tacgtttttg actgtgcgct ttaagcatgt 6540 tcgagttatt gtctctgata atgctgcgaa gatgcttcct gttgctgcta ttacacaatt 6600 gtgtgagaaa gtgtatactg atgaagtttc ctttacagat aagcaaaaga atcacatagc 6660 tttaactcgc tgggcagaca taacagttgt cttacctgct acagcaaata taattggaaa 6720 agttgctaat ggtattgcag ataactttat gacaacaact cttctttctt ctagcaagcc 6780 agttttaatt tatccttgca tgaataatat tatgtgggaa aatccagtag ttcaaaaaaa 6840 tgttgaagtt ttatctggaa cccaatataa ggtaattgtt ggacaagaat cagaatcttt 6900 tgaattagcc agtggaaaga tgaaaaagaa tattgcaatt ccaagtttgg atgaattgca 6960 acgagttgtt ttagaaaatt tacaagaaga gaggtaagag tatgaagaag aaaggattac 7020 tagtaataat ctttctaact ttctttttct tttatcctaa agctaaagct gctgaatata 7080 caattatatc aaataatagt gaacaaactg ttaatgactt gaataattta ggagttacag 7140 tcaatagcca tattgcggaa attggatata ttgaagctca aggagatgtt aacattgatc 7200 agattaaaaa gctgtcaaat attcaaagta tccagaatat ggctgataca tcacagaata 7260 tcacgactag agttccttca acatatatta accagacaat acaattgcct cagctttttt 7320 cttatcagtg ggatatgcaa aaaattacta ataatggtgt ttcatattca ttaaataaag 7380 aaaatcgaaa aaatgtaaca gttgctttag ttgattctgg gattgatgta gaccataatg 7440 cttttacagg aatgattgat agtcgttcaa aaaattttgt gcctgctgga ggatatgata 7500 atagtgaaag cagtgaaact ggaaatatta atgatattga tgataaaaaa ggccatggaa 7560 cagcagttgc tgggcaaatt gctgcaaatg gtcaaatctt tggtgtgtcc ccaggaacga 7620 accttcttat ctatagagtt tttggaaaat caaaatcaaa ggagtgctgg attttaaaag 7680 caattattga tgcaacaaat aacggtgcta atgttattaa tctaagtttg gggcaatata 7740 ttaagattcc taatggtgat atttgggagt ctgccgaagc attaggatat aagtttgcca 7800 ttgattatgc cacaagacat aatgtcattg ttgtagcagc cacaggtaat gatggattaa 7860 gtgatgacaa cggagaggtt aaaacttatt ataatagtca gcattcagga caagatatgt 7920 ctcaaaatga cacggttgaa gattatcctt ctgttttacc taatgctatt gcagttggct 7980 cttctgataa taataatcaa agatcatctt ttagtaatta ctataatcaa tatcaggaca 8040 attttatttt ggctcctggt ggtggaacaa ctttactaga ccaatatggt caagaagagt 8100 ggtataatca gaaacttttt atgaaagaac aagtcttatc aacaagtaat aatggaaatt 8160 atgattatgc agatggtact tctatttcaa caggaaaagt ttctggagag cttgcagaaa 8220 ttattagtaa ctaccatctt caaggagatt cttcaaaagc tagaagtatt ctactaaatc 8280 aagttaatta tactagtgat ggttataaag aaataagcac ttacaaagct ttgcgaggtt 8340 actaaatgaa gtggttagaa gttttgcaaa ttagtaaaaa agaaaaaatt ctttatctta 8400 ttggttgtat attttcaatt atgacaggct taattactct acgaatcacc tacttactta 8460 agaatttagt tgacagcaaa tcgtctttta ataatttgtt cttgtttctt gttttgggat 8520 tagttctttt tatcatagat gctggttcac agtatctaat ttcattgatt ggtaatcaag 8580 tagtgtttaa cagtcgaaat aatatttgga aaaaaatttc tgattggaca gatagtaaag 8640 atgattcttc tgaaatggca ggccacctta ttaatgatag tgaactgata gaaaatttta 8700 taatttctac tattcctcaa tcaataaatt cagttattgt tggatcagga tccttagtta 8760 tgctatttgt tattaatagt aaaatgtctt tagaagttat agggatttgc ttgcttttat 8820 tgttcattat gcaacccttt tctagaatat taagcaaaat aagtaaaaga atccaggaag 8880 acaaagctga acttattaat attgcctcac agttgagagg acaagtcaaa acaataaaaa 8940 gctataatgc tcaagattat gcctttcaaa aatttgatga gcaaaatcgc caattatttc 9000 aagatatctt aaatagaata aaaattttta gcatttactc tcctttttta aatatcttaa 9060 ttctttttat gattataatt gttgtttggc taggaaatac agaagtacgt tcaggaaatc 9120 tcactgtagg ttcagcaact atttttgttg tttatatgac acaattaatt aatccaatta 9180 tgcaattatc acaattagtt gctcatatgg ggatgcttaa tggcggcgtg gaacgtcttt 9240 tggagtataa tcaagctatt ccagaaaaaa atggaatcaa gaaaattgat gaaataatta 9300 atatcgcgtt tgataatgtt tcatttgctt atgataacca agaaaatatt attgaaaatg 9360 tgaatttaac ttttcaaaaa ggtacttata tttccattgt tggtgaaagt ggagttggga 9420 aatcaacctt acttgatctt ttagaacata attatgtacc atcaaaagga cgaatcttaa 9480 taaacggaat agacttagaa gaattgaata ttaagacttt gcgaaataag ataagctatg 9540 tatctcaaga accaacaatt ctttctggga caattcgtga actattagac tttaatcagc 9600 aacagcatac agaaactagt ctttggaatg ttcttgatac tgtagaatta tcagaactta 9660 ttagaaattt acccgcgaaa ttagattcta aggttgatga atatggtggt aacctctctg 9720 gaggtcagat gcaacggatc tcacttgcaa gaggattact gaaagcagga gatgttttat 9780 tattagatga atcttttgcc aatattgatg aagagacttg tcttaaaata aaattaaaaa 9840 ttgctgctta tgctgaatca cacaagcaaa ttgttattga agttattcat aatctaaata 9900 gaataactcc cagtagtatc gtttaccgat tggctgataa aaaactagaa attttgagga 9960 gcggatttta atagaaaagt cgaagaaatc tgagtaaaag atcagtttct ggtcgaaaat 10020 taaatattgt gatatataaa taagcttaaa atcaatattc ctaataattt gattttaagc 10080 tttttactat ttgatgagtt tttactcaag atcttttgat tttcctgata aagtccttaa 10140 atttgttttt tatactaaaa gcagaaaagg aggatatcat aatggattat atgctagaga 10200 cgaaaaattt aactaaacag tttggtaagc aaacagcggt taaccaattg aatttgaaag 10260 ttgaacgtca ttcaatttat ggtttgctgg ggcctaatgg ttccggcaaa tcaacaacac 10320 ttaaaatgat tactggaatg ctaagaaaga catctggtca cattcttata gacggacacg 10380 attggagccg caaggattta gaaaatatcg gggctctgat tgaatcaccg ccgctttatg 10440 aaaacctgac tgcgcgtgaa aatttaaagg taagaacctt gatgctgggt ttacctgata 10500 gtcgcattga tgaggtttta aaaatagtgg atctaaccaa cacgggtaaa aaaagagcag 10560 ggcaattttc tatgggcatg aagcagcgtc tgggtattgc tatcgcactt ttgaactcac 10620 ctcaactttt gattctggat gaaccgacta atggacttga tcctattggt attcaggagt 10680 tgcgtaatct tattcgttcc ttccctacac aaggaattac agttattatt tccagtcata 10740 tcttatctga gattcagatg acagcggatc atattggtat cattgctaat ggcgtactgg 10800 gttatcagga tagaattcac caagatgaag acttggaaaa actttttact gatgtggtta 10860 tgagataccg aggaggtgag tgatatgctg ggcatgtttc aggcagaaag gttaaaactg 10920 aagcgaagta tggcgaagaa gttactagtt tttgccccca taatagctat tttatatggt 10980 tttatagcac ctgtggggta tttagtaaat aatgcttata attggtggta tgtcatgatt 11040 tttccagggc tgctaacctt atttgctgct ttaataaata cttacgaaga aaaaaagctg 11100 cattatcgag cagtgtttcc tttgcccatt tctttaagaa aattttggtt tgaaaaaatt 11160 tttataactg tttattatct taattttagt aatggagtac tttggataat tacagtatta 11220 ctgaatactt ttattttacc aaattatgga aaagactata cttatactgt tggagaatta 11280 gcactagctt ctttggttat aatagttact acactttggc aaattccatt ttgtctgtgg 11340 ctgacaaaaa gaatcggttt taccataacg ttgataatta atttaatgag taatttcatt 11400 ttgggagttg tttttgcaac tacttcctgc tggtggcttt gtccatatag ttggggaata 11460 cgattaatgg tacccatttt aaaaatacta ccgagtggtc taaaggcagg tatagcagga 11520 gctccatcat tgccaacaag tttttggagt atcgttatta gtttgtgttt agcggttatc 11580 ttatttgtta gtttgacagt tttgagtgca tcttggtttg aaaaacagga agtgaaatga 11640 tgattgattt attaaaagca gaaaatgtaa aataccgtca tactttttta ccatggttac 11700 acctgatttt acctgttact acagctattg ttgttattgt ttatgggcta atgacgccga 11760 ctcactcttg ggctgatatt actggtggtt acttagaact attgggtata agttttccaa 11820 ttgtcattgc tgttatttgt gggaaatcag ttggactaga agtagaggct ggtcaatttc 11880 aagttatgtt agcaattaag caaaggaact tgatattttg tatcaagtta ttgaatttgc 11940 tcattttaga acttttttca actctattag ctataggaat ttatggatta atttatcaat 12000 taagtaataa acatttgata ttttatggat atgctgtaat tttactaaca gcttcaatgc 12060 tcattcttta tctgattcac ttagttgtag tatttttgtt tggcaatagt gctaatattg 12120 ggttggggat tgctgaatct ttactatctg ctttgctctt gacaggttta ggagatggta 12180 tctggcaatt tattccttgt gcttggggta ctcgcctaat gggtacctta ataaatctgt 12240 ggtattactc tgggcacagc ttatttttta agcaacagct tttaatttgg ctggaagtcg 12300 cagttccact aactttaatg gctttaatcc ttagtataat ttggttcgac agatggcaag 12360 gacgtagcag tgatgaataa aggaaaaagg agaactttca aacatgacct atattggtgt 12420 tagtcatctc aaaaaggtgt ataaaactca ggaaggcctc actaacgaag cgttaaaaga 12480 tattacgttc tcagttcaag aaggggaatt tattgctatt atgggtgaat ctggctcagg 12540 gaagtcaact ctccttaata tcctagcttg tatggattat ccaagtagtg gtcatatcat 12600 cttcaataac tatcaattag agaaagttaa agatgaagag gctgctgttt ttagaagtcg 12660 gcatattggt tttatttttc aaaatttcaa tcttttaaat atcttcaata ataaagacaa 12720 tctgttgata ccagttatta tttcgggaag taaggtgaat tcctatgaaa aacgattacg 12780 tgatttagct gctgttgttg gtatagaatc tttgctatct aaatatcctt atgaattatc 12840 tggaggtcaa caacaaaggt tagctattgc cagagcttta attatgaatc cagacttgat 12900 attggccgat gagccaacag gacaattgga ctctaagact tctcagcgaa tcttgaattt 12960 gttgtctaac atcaacgcta aacgaaagac aattctaatg gtgactcata gtcctaaagc 13020 tgctagttat gcaaaccgag ttctttttat caaggatggt gttattttca atcaacttgt 13080 tcgtgggtgt aaatccaggg aaggcttttt agatcaaatt attatggctc aggccagtct 13140 gtaggaggtt gtcctgatta tgtttttacc caaaatttcc tttcataatc ttattgtaaa 13200 taaatcatta accttacctt attttgctat tatgaccatt tttagtggtt ttaactatgt 13260 tttgattaat tttttaacca accctagttt ttataacatt ccaacagcta ggatactgat 13320 tgatattctt atttttggtt ttatcttaat ttcattactg atgttgcttt atggtcgcta 13380 tgccaatcgt tttataagtg atgagcgtaa tagtaatatg ggaatttttc tcatgttggg 13440 aatggggaaa aagcaattat taaaaataat ctatttggaa aagttatatc tttttacagg 13500 aacgtttttt ggaggtttaa tctttggttt cgtatacagt aagatatttt ttctttttat 13560 cagaaatcta attgttattg gagatgtcag agaacaatat agcttaacgg ctattagttg 13620 gctacttatt cttacttttt ttatttattt tattatttat ctatcagagt accgattatt 13680 aaaacgtcaa agtatcacgg ttatttttaa tagcaaagct aagcgtgata atcctagaaa 13740 aactagtgtt tttgttggac tttttggact ttttgccctg ttaatgggat atcattttgc 13800 tttaacaagt cccaatgtca caaccagttt cagccgtttc atttatgctg cctgcttagt 13860 tactctaggt attttttgca cgttttcgtc aggtgtgatt atgttactga ctgtcataaa 13920 gaagagaaga gctatctact ataatcaacg gcgctttgtt gtgattgcta gtttatttca 13980 ccgtatccgc agtaatgctc tgtctttggc gactatctgt atttttagca ccgctacctt 14040 agttagttta tctgtcttag ctagtctcta tcttgcaaag gacaatatgg ttcgtctttc 14100 aagtcctaga gatgttacgg tgctatctac aactgatatt gaaccgaatt taatggacat 14160 cgctacaaaa aatcatgtta ctctaactaa tcgccagaat ttaaaggttt ctcaatctgt 14220 ttatggtaat atcaaaggaa gtcatttgtc agttgatcct aatggcggta tggctaatga 14280 ttatcaaata acagttattt cattggattc ttttaatgct tctaataata cccattatcg 14340 tttaaaaaat catgaaattc tcacctatgt ttcaaatgga gcagctgctc cctctagcta 14400 tacaactaat ggtgttaaac taaccaatgt taaacaaatt aaaaggataa actttatttt 14460 ttctccgcta cgctctatgc agcctaattt ctttataatt actgacaatc gagaaataat 14520 tcagactatt ttgaaagagg agctaacatg gggaacgatg gcaggctacc atgttaaagg 14580 aaaaaaaatg aatcagaaag atttttatga tgagcttgag actactaatt tcaggcaatt 14640 tagtgctaat gtagtttcaa taagacaggt caaatcaatg tttaatgctt tatttggcgg 14700 tttactcttt gttggtatta tttttggaac tatttttgca attttgacag ctataactat 14760 ttattatcaa cagctttctg aaggaattcg agaccgagat gattataagg ccatgataaa 14820 attaggtatg acaaataaaa ctattcaaga cagtattaag gttcaaataa actttgtttt 14880 catcttgccc attgcttttg ccctattaaa tctcatcttt gcacttccta ttttatataa 14940 aataatgaca acttttggat ttaatgatgc aggactattt ctaagagctg ttggaacttg 15000 tctgattgtt taccttttct tttattggtt tatttgtcat tgcacatcca aactatatta 15060 tcgtttaata tctaaaaaat agaggagttt atattatgcg tattgtaagt tcattggtat 15120 cgcttttatt gactatcttt tggatttttg ctatagcttt tatcccaatt ggagaccaga 15180 atagttttaa taaaccagaa atgtggttct ttgttttttt cgctattatt atttatagta 15240 ttgttataat aagcgattat tatctaaaga gctttaatct tttgaaagtt tatcaaattt 15300 tagttttgtt tattagcata ctgtgtgctc tttgtggttt atcactaact gctttaggat 15360 tgaaagtatt cactttagct attggaattg ttagtcttgt taatacaatt atttatttct 15420 ttttcgctaa taaaaaagat aatgttgaat aaaatatgtt atcctagtga aggaggtttc 15480 ctagaatgac ccgtattttg gtaattgatg atgatgcaga tattttggct ctgataaaaa 15540 ataccttgca actgcaaaac tatctgg 15567 4 289 PRT Streptococcus mutans 4 Leu Lys Val Asn Gln Ser Met Glu Leu Gly Glu Leu Tyr Arg Glu Leu 1 5 10 15 Arg Ile Ala Arg Gly Leu Lys Ile Lys Asp Ile Ala Cys Lys Asn Leu 20 25 30 Ser Lys Ser Gln Leu Ser Arg Phe Glu Asn Gly Gln Thr Met Leu Ala 35 40 45 Ala Asp Lys Leu Leu Leu Ala Ile Ser Gly Ile His Met Ser Phe Ser 50 55 60 Glu Phe Gly Tyr Ala Leu Ser His Tyr Glu Glu Ser Asp Phe Phe Lys 65 70 75 80 Arg Gly Asn Lys Leu Ser Glu Leu Tyr Val Gln Lys Asp Ile Lys Gly 85 90 95 Leu Lys Lys Leu Leu Glu Phe Asn Asp Asn His Glu Val Phe Asp Val 100 105 110 Tyr Asn Arg Leu Asn Lys Leu Val Ile Gln Val Thr Ile His Leu Leu 115 120 125 Asp Thr Asp Tyr Ile Ile Ser Asp Asp Asp Lys Asn Phe Leu Thr Thr 130 135 140 Tyr Leu Tyr Asn Ile Glu Glu Trp Thr Glu Tyr Glu Leu Tyr Ile Phe 145 150 155 160 Gly Asn Thr Met Ser Ile Leu Ser Ser Asp Asp Leu Ile Phe Leu Gly 165 170 175 Lys Ala Phe Val Glu Arg Asp Lys Leu Tyr Ile Ser Leu Pro Ser His 180 185 190 Lys Lys Asn Ala Glu Leu Thr Phe Leu Asn Leu Ile Leu Ile Leu Leu 195 200 205 Glu Arg Lys Lys Leu Tyr Gln Ala Ile Tyr Phe Val Glu Asn Leu Glu 210 215 220 Lys Leu Leu Asn Tyr Gln Asp Met Phe Ala Ile Thr Phe Leu Lys Phe 225 230 235 240 Leu Lys Lys Ile Ile Thr Tyr Phe His Asp Lys Ser Val Asp Met Ser 245 250 255 Glu Leu Glu His Tyr Ile Asn Ile Val Glu Glu Ile Asn Pro Thr Ile 260 265 270 Ala Ser Ile Leu Lys Ser Asn Leu Asn Gln Leu Leu Ser Ser Phe Ser 275 280 285 His 5 65 PRT Streptococcus mutans 5 Met Ser Asn Thr Gln Leu Leu Glu Val Leu Gly Thr Glu Thr Phe Asp 1 5 10 15 Val Gln Glu Asp Leu Phe Ala Phe Asp Thr Thr Asp Thr Thr Ile Val 20 25 30 Ala Ser Asn Asp Asp Pro Asp Thr Arg Phe Ser Ser Leu Ser Leu Cys 35 40 45 Ser Leu Gly Cys Thr Gly Val Lys Asn Pro Ser Phe Asn Ser Tyr Cys 50 55 60 Cys 65 6 64 PRT Streptococcus mutans 6 Met Leu Asn Thr Gln Leu Leu Glu Val Leu Gly Thr Lys Thr Phe Asp 1 5 10 15 Val Gln Glu Asp Leu Phe Glu Phe Asn Ile Thr Asp Thr Ile Val Leu 20 25 30 Gln Val Ser Asp Ser Pro Gly Thr His Ser Lys Val Gly Ser Phe Ser 35 40 45 Ile Cys Pro Pro Arg Lys Thr Ser Val Ser Phe Asn Ser Tyr Cys Cys 50 55 60 7 990 PRT Streptococcus mutans 7 Met Asn Asp Phe Gln Phe Gln Asp Tyr Phe Met Tyr Arg Lys Pro Leu 1 5 10 15 Gly Asn Phe Ser Asn Phe Leu Ser Ile Thr Asp Met Met Asp Pro Ile 20 25 30 Glu Leu Leu His Asn Asp Pro Ile Phe Ala Glu Gly Val Tyr Leu Ala 35 40 45 Ser Pro Ser Leu Arg Ser Ser Ile Asn Lys Leu Glu Asn Gln Ile Ala 50 55 60 Ser Thr Lys Glu Lys Lys Asn Ala Lys Glu Thr Ile Phe Gln Tyr Tyr 65 70 75 80 Ala Arg Tyr Asn Thr Arg Ser Thr Pro Phe Gly Leu Phe Ser Ser Ile 85 90 95 Gly Ile Gly Gly Phe Ser Asn His Pro Arg Lys Glu Lys Ser Cys Tyr 100 105 110 Glu Lys Ser Val Asn Val Asp Leu Phe Trp Ala Tyr Lys Val Ala Asp 115 120 125 Lys Leu Glu Ser Met Pro Glu Ile Leu Asn Thr Leu Lys Val Val Ala 130 135 140 Asn Asn Ala Leu Gln Lys Ser Asn Asp Phe Trp Leu Leu Asp Thr Arg 145 150 155 160 Ser His Phe Gly Leu Met Asn Ser Arg Ser Asp Ile Arg Glu Asp Ile 165 170 175 Thr Val Lys Ser Asn Gln Leu Ile Asp Tyr Val Ile Asn Cys Thr Glu 180 185 190 Glu Pro Ile Ser Tyr Gln Thr Leu Ile Asp Asp Ile Ala Glu Lys Phe 195 200 205 Ser Gln Ser Ser Asp Asp Val Lys Glu Tyr Leu Gln Thr Leu Ile Lys 210 215 220 Glu Glu Phe Leu Ile Thr Glu Leu Lys Phe Ser Leu Ile Asp Asp Asn 225 230 235 240 Pro Leu Asp Trp Phe Ile Asn Ile Leu Glu Arg Asp Gln Asn Asn Ser 245 250 255 Glu Leu Leu Glu Lys Leu Thr Glu Ile Lys Ala Met Ile Gln Asp Tyr 260 265 270 Thr Asp Arg Asn Ile Gly Glu Gly Asn Asn Ser Ile Leu Ala Leu Glu 275 280 285 Asn Lys Met Ser Gln Ile Val Lys Ala Asn Ala Tyr Leu Arg Val Asp 290 295 300 Leu Tyr Asp His Ala Glu Leu Lys Leu Ala Gln His Thr Lys Ser Ser 305 310 315 320 Leu Gln Asn Ile Leu Lys Val Leu Ser Ser Phe Ser Ser Ala Val Asn 325 330 335 Ser Gln Lys Glu Ile Lys Asn Tyr His Glu Lys Phe Ile Ala Arg Tyr 340 345 350 Gly Tyr Glu Gln Leu Val Pro Leu Gln Leu Leu Leu Asn Ser Thr Ser 355 360 365 Gly Leu Gly Phe Pro Lys Gly Tyr Ser Gln Thr Glu Val Ser Lys Gln 370 375 380 Asn Asn Glu Asp Ser Lys Asn Gln Lys Ile Ile Glu Phe Leu Gln Arg 385 390 395 400 Lys Phe Glu Lys Ala Leu Arg Asp Gly Lys Glu Ile Ile Leu Ser Asp 405 410 415 Asp Asp Leu Lys Asp Leu Asn Phe Asp Thr Glu Gln Gln Ile Ser Gly 420 425 430 Glu Leu Tyr Cys Phe Tyr Asn Phe Lys Ser Lys Lys Leu Glu Val Ser 435 440 445 Ser Leu Gly Val Ser Gln Met Leu Gly Asn Thr Phe Gly Arg Phe His 450 455 460 Ser Lys Leu Pro Asn Thr Ile Val Thr Lys Asn Val Asn Lys Thr Lys 465 470 475 480 Glu Ile Phe Thr Glu Ala Tyr Pro Asn Thr Ile Ile Thr Gln Leu Asn 485 490 495 Glu Val Pro Tyr Phe Gly Arg Gly Gly Asn Ile Met Ile Ser Asn Ser 500 505 510 Leu Lys Ser His Gln Leu Glu Leu Arg Asn Tyr Thr Thr Lys Lys Glu 515 520 525 Met Ser Ile Asn Asp Ile Tyr Val Arg Ala Thr Ser Glu Glu Leu Tyr 530 535 540 Phe Tyr Ser Lys Lys Tyr Glu Lys Arg Val Ile Phe Val Met Asn Asn 545 550 555 560 Met Phe Asn Tyr Ile Asn Gly Ser Lys Leu Leu Arg Phe Leu Leu Glu 565 570 575 Val Ser Asn Ser Asp Phe Gln Asn Ile Thr Pro Ile Thr Leu Gly Ser 580 585 590 Leu Asp Ser Tyr Asn His Val Pro Ala Ile Ile Tyr Lys Asp Ile Ile 595 600 605 Ile Lys Pro Glu Thr Trp Asn Ile Arg Lys Ser Glu Ala Lys Thr Leu 610 615 620 Asp Ser Leu Lys Asn Trp Leu Thr Asn Asn Asn Val Pro Pro Phe Val 625 630 635 640 Arg Met Lys Tyr Thr Asp Gln Ile Ile Tyr Leu Asp Leu Ser Arg Thr 645 650 655 Ile Asp Leu Thr Met Leu Phe Gln Ser Ile Lys Lys His Ser Phe Ile 660 665 670 Gln Leu Leu Asp Val His Ser Val Cys Thr Asn Asp Thr Glu Ile Leu 675 680 685 Glu Leu Val Val Pro Phe Thr Arg Ser Asp Val Asn Ala His Gln Ile 690 695 700 Tyr His Tyr Ala Gln Asn Ile Tyr Thr Leu Glu Asp Ser Gly Ser Lys 705 710 715 720 Glu Lys Tyr Phe Tyr Ala Lys Ile Tyr Val Asn Lys Gln Arg Gln Thr 725 730 735 Ser Phe Leu Gln Lys Glu Tyr Pro Leu Leu Leu Lys Tyr Leu Lys Leu 740 745 750 Pro Glu Asn Leu Gln Trp Phe Tyr Ile Arg Tyr Lys Asp Asp Gly Lys 755 760 765 Asp Ser Ile Arg Leu Arg Ile Arg Tyr Val Glu Asp Lys Gln Leu Val 770 775 780 Gln Leu Tyr Ser Arg Phe Ile Glu Trp Ala Thr Lys Ala Arg Lys Asn 785 790 795 800 Ile Gln Ile Ser Gly Tyr Glu Ile Ser Glu Tyr Ile Pro Glu Ser Ala 805 810 815 Arg Tyr Gly Gly Lys Lys Tyr Ser Ser Ile Ile His Ser Phe Phe Tyr 820 825 830 Tyr Asp Ser Ile Leu Asp Leu Leu Leu Gln Lys Lys Ala Glu Gln Thr 835 840 845 Ile Glu Val Arg Thr Ser Leu Ser Ile Ile Arg Met Phe Leu Met Met 850 855 860 Lys Leu Ser Leu Gln Asp Gln Gln Lys Leu Ile Lys Asn Leu Phe Asp 865 870 875 880 Gly Lys His Lys Leu Lys Tyr Glu Lys Glu Tyr His Asn Ser Ile Ser 885 890 895 Leu Leu Leu Asp Asn Leu Cys Thr Lys Asn Gln Thr Asp Glu Ala Asp 900 905 910 Ile Phe Cys Val Met Asn Met Lys Lys Ile Thr Glu Lys Ile Ser Ser 915 920 925 Val Leu Lys Gln Lys Asp Leu Thr Thr Asp Trp Gln Arg Ile Leu Gly 930 935 940 Ser Leu Ile His Met Arg Cys Asn Arg Val Tyr Gly Ile Asn Ser Glu 945 950 955 960 Leu Glu Arg Lys Thr Met Phe Ile Val Asp Lys Val Ile Asn Ser Lys 965 970 975 Arg Tyr Thr Asp Met Phe Leu Glu Val Gly Asn Glu Thr Lys 980 985 990 8 424 PRT Streptococcus mutans 8 Met Arg Gln Ser Lys Arg Val Glu Lys Ile Lys Asp Ile Leu Thr Glu 1 5 10 15 Gln Thr Tyr Leu Phe Asp Tyr Gln Glu Ile Leu Lys Lys Val Ser Gln 20 25 30 Ala Lys Gln Thr Asp Phe Trp Asn Leu Leu Ser Leu Ser Ser Gly Ile 35 40 45 Thr Ser Leu Leu Ile Phe Tyr Gln Glu Tyr Glu Asn Leu Glu Gly Val 50 55 60 Asn Leu Lys Gln Gln Lys Gln Ser Leu Ile Gly Leu Ile Ser His Tyr 65 70 75 80 Ile Asn Gln Ile Ala Glu Lys Ser Ser Leu Phe Asp Gly Leu Ala Gly 85 90 95 Val Gly Phe Ala Ile Asn Tyr Ile Ser Asn Asn Gly Lys Tyr Tyr Gln 100 105 110 Lys Leu Leu Glu Gln Ile Asp Asn Arg Leu Arg Gln Asn Ile Glu Arg 115 120 125 Asn Leu Val Asn Tyr Lys Asn Glu Glu Tyr Ala Asn Pro Met Asn Tyr 130 135 140 Asp Val Val Ser Gly Asn Ala Gly Val Ala Arg Tyr Leu Met Glu Arg 145 150 155 160 Glu Ser Ser Glu Asp Trp Arg Ile Val Glu Met Ile Leu Glu Thr Phe 165 170 175 Tyr Lys Ala Leu Glu Gln Gly Trp Arg Val Gln Ser Lys Tyr Gln Phe 180 185 190 Leu Glu Ser Glu Lys Gln Tyr Tyr Leu Glu Gly Asn Ile Asn Phe Gly 195 200 205 Leu Ala His Gly Ile Leu Gly Pro Ala Thr Ile Met Ala Leu Tyr Gln 210 215 220 Arg Arg Glu Pro Gln Asn Thr Arg Asn Ala Glu Lys Leu Gln Glu Thr 225 230 235 240 Tyr Arg Leu Ile Lys Arg Tyr Ala Gln Val Arg Asp Glu Gly Leu Arg 245 250 255 Trp Pro Ile Arg Tyr Asp Leu Phe Arg Lys Glu Gly Ser Phe Ile Leu 260 265 270 Arg Asn Gly Trp Cys Tyr Gly Glu Asn Gly Ile Tyr Asn Thr Leu Phe 275 280 285 Leu Met Gly Lys Val Leu Ser Asn Gln Glu Ile Cys Glu Thr Ala Gln 290 295 300 Lys Val Ile Pro Ser Ile Ile Lys Asp Asp Tyr Glu Lys Met Glu Ser 305 310 315 320 Pro Thr Phe Cys His Gly Phe Ala Gly Lys Ala Asn Phe Phe Leu Leu 325 330 335 Gln Tyr Gln Arg Thr Lys Glu Ser Ile Phe Leu Val Lys Ala Glu Glu 340 345 350 Glu Ile Asp Lys Ile Leu Ile Val Tyr Asn Ser Glu Asn Met Phe Gly 355 360 365 Phe Lys Asp Ile Glu Asp Asn Ile Asp Asn Thr Gly Glu Arg Leu Thr 370 375 380 Tyr Trp Asp Asn Phe Gly Leu Leu Ser Gly Thr Val Gly Val Leu Leu 385 390 395 400 Val Leu Met Glu Tyr Cys Asn Ile Val Asn Ala Gly Lys Ile Ala Glu 405 410 415 Trp Asn Lys Ile Phe Leu Leu Thr 420 9 188 PRT Streptococcus mutans 9 Met Glu Glu Gln Asn Ile Glu Lys Lys Ile Leu Leu Cys Leu Thr Gly 1 5 10 15 Ser Gly Ala Leu Leu Gly Ile Ala Glu Tyr Ile Thr Phe Leu Thr Val 20 25 30 Arg Phe Lys His Val Arg Val Ile Val Ser Asp Asn Ala Ala Lys Met 35 40 45 Leu Pro Val Ala Ala Ile Thr Gln Leu Cys Glu Lys Val Tyr Thr Asp 50 55 60 Glu Val Ser Phe Thr Asp Lys Gln Lys Asn His Ile Ala Leu Thr Arg 65 70 75 80 Trp Ala Asp Ile Thr Val Val Leu Pro Ala Thr Ala Asn Ile Ile Gly 85 90 95 Lys Val Ala Asn Gly Ile Ala Asp Asn Phe Met Thr Thr Thr Leu Leu 100 105 110 Ser Ser Ser Lys Pro Val Leu Ile Tyr Pro Cys Met Asn Asn Ile Met 115 120 125 Trp Glu Asn Pro Val Val Gln Lys Asn Val Glu Val Leu Ser Gly Thr 130 135 140 Gln Tyr Lys Val Ile Val Gly Gln Glu Ser Glu Ser Phe Glu Leu Ala 145 150 155 160 Ser Gly Lys Met Lys Lys Asn Ile Ala Ile Pro Ser Leu Asp Glu Leu 165 170 175 Gln Arg Val Val Leu Glu Asn Leu Gln Glu Glu Arg 180 185 10 447 PRT Streptococcus mutans 10 Met Lys Lys Lys Gly Leu Leu Val Ile Ile Phe Leu Thr Phe Phe Phe 1 5 10 15 Phe Tyr Pro Lys Ala Lys Ala Ala Glu Tyr Thr Ile Ile Ser Asn Asn 20 25 30 Ser Glu Gln Thr Val Asn Asp Leu Asn Asn Leu Gly Val Thr Val Asn 35 40 45 Ser His Ile Ala Glu Ile Gly Tyr Ile Glu Ala Gln Gly Asp Val Asn 50 55 60 Ile Asp Gln Ile Lys Lys Leu Ser Asn Ile Gln Ser Ile Gln Asn Met 65 70 75 80 Ala Asp Thr Ser Gln Asn Ile Thr Thr Arg Val Pro Ser Thr Tyr Ile 85 90 95 Asn Gln Thr Ile Gln Leu Pro Gln Leu Phe Ser Tyr Gln Trp Asp Met 100 105 110 Gln Lys Ile Thr Asn Asn Gly Val Ser Tyr Ser Leu Asn Lys Glu Asn 115 120 125 Arg Lys Asn Val Thr Val Ala Leu Val Asp Ser Gly Ile Asp Val Asp 130 135 140 His Asn Ala Phe Thr Gly Met Ile Asp Ser Arg Ser Lys Asn Phe Val 145 150 155 160 Pro Ala Gly Gly Tyr Asp Asn Ser Glu Ser Ser Glu Thr Gly Asn Ile 165 170 175 Asn Asp Ile Asp Asp Lys Lys Gly His Gly Thr Ala Val Ala Gly Gln 180 185 190 Ile Ala Ala Asn Gly Gln Ile Phe Gly Val Ser Pro Gly Thr Asn Leu 195 200 205 Leu Ile Tyr Arg Val Phe Gly Lys Ser Lys Ser Lys Glu Cys Trp Ile 210 215 220 Leu Lys Ala Ile Ile Asp Ala Thr Asn Asn Gly Ala Asn Val Ile Asn 225 230 235 240 Leu Ser Leu Gly Gln Tyr Ile Lys Ile Pro Asn Gly Asp Ile Trp Glu 245 250 255 Ser Ala Glu Ala Leu Gly Tyr Lys Phe Ala Ile Asp Tyr Ala Thr Arg 260 265 270 His Asn Val Ile Val Val Ala Ala Thr Gly Asn Asp Gly Leu Ser Asp 275 280 285 Asp Asn Gly Glu Val Lys Thr Tyr Tyr Asn Ser Gln His Ser Gly Gln 290 295 300 Asp Met Ser Gln Asn Asp Thr Val Glu Asp Tyr Pro Ser Val Leu Pro 305 310 315 320 Asn Ala Ile Ala Val Gly Ser Ser Asp Asn Asn Asn Gln Arg Ser Ser 325 330 335 Phe Ser Asn Tyr Tyr Asn Gln Tyr Gln Asp Asn Phe Ile Leu Ala Pro 340 345 350 Gly Gly Gly Thr Thr Leu Leu Asp Gln Tyr Gly Gln Glu Glu Trp Tyr 355 360 365 Asn Gln Lys Leu Phe Met Lys Glu Gln Val Leu Ser Thr Ser Asn Asn 370 375 380 Gly Asn Tyr Asp Tyr Ala Asp Gly Thr Ser Ile Ser Thr Gly Lys Val 385 390 395 400 Ser Gly Glu Leu Ala Glu Ile Ile Ser Asn Tyr His Leu Gln Gly Asp 405 410 415 Ser Ser Lys Ala Arg Ser Ile Leu Leu Asn Gln Val Asn Tyr Thr Ser 420 425 430 Asp Gly Tyr Lys Glu Ile Ser Thr Tyr Lys Ala Leu Arg Gly Tyr 435 440 445 11 541 PRT Streptococcus mutans 11 Met Lys Trp Leu Glu Val Leu Gln Ile Ser Lys Lys Glu Lys Ile Leu 1 5 10 15 Tyr Leu Ile Gly Cys Ile Phe Ser Ile Met Thr Gly Leu Ile Thr Leu 20 25 30 Arg Ile Thr Tyr Leu Leu Lys Asn Leu Val Asp Ser Lys Ser Ser Phe 35 40 45 Asn Asn Leu Phe Leu Phe Leu Val Leu Gly Leu Val Leu Phe Ile Ile 50 55 60 Asp Ala Gly Ser Gln Tyr Leu Ile Ser Leu Ile Gly Asn Gln Val Val 65 70 75 80 Phe Asn Ser Arg Asn Asn Ile Trp Lys Lys Ile Ser Asp Trp Thr Asp 85 90 95 Ser Lys Asp Asp Ser Ser Glu Met Ala Gly His Leu Ile Asn Asp Ser 100 105 110 Glu Leu Ile Glu Asn Phe Ile Ile Ser Thr Ile Pro Gln Ser Ile Asn 115 120 125 Ser Val Ile Val Gly Ser Gly Ser Leu Val Met Leu Phe Val Ile Asn 130 135 140 Ser Lys Met Ser Leu Glu Val Ile Gly Ile Cys Leu Leu Leu Leu Phe 145 150 155 160 Ile Met Gln Pro Phe Ser Arg Ile Leu Ser Lys Ile Ser Lys Arg Ile 165 170 175 Gln Glu Asp Lys Ala Glu Leu Ile Asn Ile Ala Ser Gln Leu Arg Gly 180 185 190 Gln Val Lys Thr Ile Lys Ser Tyr Asn Ala Gln Asp Tyr Ala Phe Gln 195 200 205 Lys Phe Asp Glu Gln Asn Arg Gln Leu Phe Gln Asp Ile Leu Asn Arg 210 215 220 Ile Lys Ile Phe Ser Ile Tyr Ser Pro Phe Leu Asn Ile Leu Ile Leu 225 230 235 240 Phe Met Ile Ile Ile Val Val Trp Leu Gly Asn Thr Glu Val Arg Ser 245 250 255 Gly Asn Leu Thr Val Gly Ser Ala Thr Ile Phe Val Val Tyr Met Thr 260 265 270 Gln Leu Ile Asn Pro Ile Met Gln Leu Ser Gln Leu Val Ala His Met 275 280 285 Gly Met Leu Asn Gly Gly Val Glu Arg Leu Leu Glu Tyr Asn Gln Ala 290 295 300 Ile Pro Glu Lys Asn Gly Ile Lys Lys Ile Asp Glu Ile Ile Asn Ile 305 310 315 320 Ala Phe Asp Asn Val Ser Phe Ala Tyr Asp Asn Gln Glu Asn Ile Ile 325 330 335 Glu Asn Val Asn Leu Thr Phe Gln Lys Gly Thr Tyr Ile Ser Ile Val 340 345 350 Gly Glu Ser Gly Val Gly Lys Ser Thr Leu Leu Asp Leu Leu Glu His 355 360 365 Asn Tyr Val Pro Ser Lys Gly Arg Ile Leu Ile Asn Gly Ile Asp Leu 370 375 380 Glu Glu Leu Asn Ile Lys Thr Leu Arg Asn Lys Ile Ser Tyr Val Ser 385 390 395 400 Gln Glu Pro Thr Ile Leu Ser Gly Thr Ile Arg Glu Leu Leu Asp Phe 405 410 415 Asn Gln Gln Gln His Thr Glu Thr Ser Leu Trp Asn Val Leu Asp Thr 420 425 430 Val Glu Leu Ser Glu Leu Ile Arg Asn Leu Pro Ala Lys Leu Asp Ser 435 440 445 Lys Val Asp Glu Tyr Gly Gly Asn Leu Ser Gly Gly Gln Met Gln Arg 450 455 460 Ile Ser Leu Ala Arg Gly Leu Leu Lys Ala Gly Asp Val Leu Leu Leu 465 470 475 480 Asp Glu Ser Phe Ala Asn Ile Asp Glu Glu Thr Cys Leu Lys Ile Lys 485 490 495 Leu Lys Ile Ala Ala Tyr Ala Glu Ser His Lys Gln Ile Val Ile Glu 500 505 510 Val Ile His Asn Leu Asn Arg Ile Thr Pro Ser Ser Ile Val Tyr Arg 515 520 525 Leu Ala Asp Lys Lys Leu Glu Ile Leu Arg Ser Gly Phe 530 535 540 12 233 PRT Streptococcus mutans 12 Met Asp Tyr Met Leu Glu Thr Lys Asn Leu Thr Lys Gln Phe Gly Lys 1 5 10 15 Gln Thr Ala Val Asn Gln Leu Asn Leu Lys Val Glu Arg His Ser Ile 20 25 30 Tyr Gly Leu Leu Gly Pro Asn Gly Ser Gly Lys Ser Thr Thr Leu Lys 35 40 45 Met Ile Thr Gly Met Leu Arg Lys Thr Ser Gly His Ile Leu Ile Asp 50 55 60 Gly His Asp Trp Ser Arg Lys Asp Leu Glu Asn Ile Gly Ala Leu Ile 65 70 75 80 Glu Ser Pro Pro Leu Tyr Glu Asn Leu Thr Ala Arg Glu Asn Leu Lys 85 90 95 Val Arg Thr Leu Met Leu Gly Leu Pro Asp Ser Arg Ile Asp Glu Val 100 105 110 Leu Lys Ile Val Asp Leu Thr Asn Thr Gly Lys Lys Arg Ala Gly Gln 115 120 125 Phe Ser Met Gly Met Lys Gln Arg Leu Gly Ile Ala Ile Ala Leu Leu 130 135 140 Asn Ser Pro Gln Leu Leu Ile Leu Asp Glu Pro Thr Asn Gly Leu Asp 145 150 155 160 Pro Ile Gly Ile Gln Glu Leu Arg Asn Leu Ile Arg Ser Phe Pro Thr 165 170 175 Gln Gly Ile Thr Val Ile Ile Ser Ser His Ile Leu Ser Glu Ile Gln 180 185 190 Met Thr Ala Asp His Ile Gly Ile Ile Ala Asn Gly Val Leu Gly Tyr 195 200 205 Gln Asp Arg Ile His Gln Asp Glu Asp Leu Glu Lys Leu Phe Thr Asp 210 215 220 Val Val Met Arg Tyr Arg Gly Gly Glu 225 230 13 251 PRT Streptococcus mutans 13 Met Leu Gly Met Phe Gln Ala Glu Arg Leu Lys Leu Lys Arg Ser Met 1 5 10 15 Ala Lys Lys Leu Leu Val Phe Ala Pro Ile Ile Ala Ile Leu Tyr Gly 20 25 30 Phe Ile Ala Pro Val Gly Tyr Leu Val Asn Asn Ala Tyr Asn Trp Trp 35 40 45 Tyr Val Met Ile Phe Pro Gly Leu Leu Thr Leu Phe Ala Ala Leu Ile 50 55 60 Asn Thr Tyr Glu Glu Lys Lys Leu His Tyr Arg Ala Val Phe Pro Leu 65 70 75 80 Pro Ile Ser Leu Arg Lys Phe Trp Phe Glu Lys Ile Phe Ile Thr Val 85 90 95 Tyr Tyr Leu Asn Phe Ser Asn Gly Val Leu Trp Ile Ile Thr Val Leu 100 105 110 Leu Asn Thr Phe Ile Leu Pro Asn Tyr Gly Lys Asp Tyr Thr Tyr Thr 115 120 125 Val Gly Glu Leu Ala Leu Ala Ser Leu Val Ile Ile Val Thr Thr Leu 130 135 140 Trp Gln Ile Pro Phe Cys Leu Trp Leu Thr Lys Arg Ile Gly Phe Thr 145 150 155 160 Ile Thr Leu Ile Ile Asn Leu Met Ser Asn Phe Ile Leu Gly Val Val 165 170 175 Phe Ala Thr Thr Ser Cys Trp Trp Leu Cys Pro Tyr Ser Trp Gly Ile 180 185 190 Arg Leu Met Val Pro Ile Leu Lys Ile Leu Pro Ser Gly Leu Lys Ala 195 200 205 Gly Ile Ala Gly Ala Pro Ser Leu Pro Thr Ser Phe Trp Ser Ile Val 210 215 220 Ile Ser Leu Cys Leu Ala Val Ile Leu Phe Val Ser Leu Thr Val Leu 225 230 235 240 Ser Ala Ser Trp Phe Glu Lys Gln Glu Val Lys 245 250 14 246 PRT Streptococcus mutans 14 Met Ile Asp Leu Leu Lys Ala Glu Asn Val Lys Tyr Arg His Thr Phe 1 5 10 15 Leu Pro Trp Leu His Leu Ile Leu Pro Val Thr Thr Ala Ile Val Val 20 25 30 Ile Val Tyr Gly Leu Met Thr Pro Thr His Ser Trp Ala Asp Ile Thr 35 40 45 Gly Gly Tyr Leu Glu Leu Leu Gly Ile Ser Phe Pro Ile Val Ile Ala 50 55 60 Val Ile Cys Gly Lys Ser Val Gly Leu Glu Val Glu Ala Gly Gln Phe 65 70 75 80 Gln Val Met Leu Ala Ile Lys Gln Arg Asn Leu Ile Phe Cys Ile Lys 85 90 95 Leu Leu Asn Leu Leu Ile Leu Glu Leu Phe Ser Thr Leu Leu Ala Ile 100 105 110 Gly Ile Tyr Gly Leu Ile Tyr Gln Leu Ser Asn Lys His Leu Ile Phe 115 120 125 Tyr Gly Tyr Ala Val Ile Leu Leu Thr Ala Ser Met Leu Ile Leu Tyr 130 135 140 Leu Ile His Leu Val Val Val Phe Leu Phe Gly Asn Ser Ala Asn Ile 145 150 155 160 Gly Leu Gly Ile Ala Glu Ser Leu Leu Ser Ala Leu Leu Leu Thr Gly 165 170 175 Leu Gly Asp Gly Ile Trp Gln Phe Ile Pro Cys Ala Trp Gly Thr Arg 180 185 190 Leu Met Gly Thr Leu Ile Asn Leu Trp Tyr Tyr Ser Gly His Ser Leu 195 200 205 Phe Phe Lys Gln Gln Leu Leu Ile Trp Leu Glu Val Ala Val Pro Leu 210 215 220 Thr Leu Met Ala Leu Ile Leu Ser Ile Ile Trp Phe Asp Arg Trp Gln 225 230 235 240 Gly Arg Ser Ser Asp Glu 245 15 246 PRT Streptococcus mutans 15 Met Thr Tyr Ile Gly Val Ser His Leu Lys Lys Val Tyr Lys Thr Gln 1 5 10 15 Glu Gly Leu Thr Asn Glu Ala Leu Lys Asp Ile Thr Phe Ser Val Gln 20 25 30 Glu Gly Glu Phe Ile Ala Ile Met Gly Glu Ser Gly Ser Gly Lys Ser 35 40 45 Thr Leu Leu Asn Ile Leu Ala Cys Met Asp Tyr Pro Ser Ser Gly His 50 55 60 Ile Ile Phe Asn Asn Tyr Gln Leu Glu Lys Val Lys Asp Glu Glu Ala 65 70 75 80 Ala Val Phe Arg Ser Arg His Ile Gly Phe Ile Phe Gln Asn Phe Asn 85 90 95 Leu Leu Asn Ile Phe Asn Asn Lys Asp Asn Leu Leu Ile Pro Val Ile 100 105 110 Ile Ser Gly Ser Lys Val Asn Ser Tyr Glu Lys Arg Leu Arg Asp Leu 115 120 125 Ala Ala Val Val Gly Ile Glu Ser Leu Leu Ser Lys Tyr Pro Tyr Glu 130 135 140 Leu Ser Gly Gly Gln Gln Gln Arg Leu Ala Ile Ala Arg Ala Leu Ile 145 150 155 160 Met Asn Pro Asp Leu Ile Leu Ala Asp Glu Pro Thr Gly Gln Leu Asp 165 170 175 Ser Lys Thr Ser Gln Arg Ile Leu Asn Leu Leu Ser Asn Ile Asn Ala 180 185 190 Lys Arg Lys Thr Ile Leu Met Val Thr His Ser Pro Lys Ala Ala Ser 195 200 205 Tyr Ala Asn Arg Val Leu Phe Ile Lys Asp Gly Val Ile Phe Asn Gln 210 215 220 Leu Val Arg Gly Cys Lys Ser Arg Glu Gly Phe Leu Asp Gln Ile Ile 225 230 235 240 Met Ala Gln Ala Ser Leu 245 16 640 PRT Streptococcus mutans 16 Met Phe Leu Pro Lys Ile Ser Phe His Asn Leu Ile Val Asn Lys Ser 1 5 10 15 Leu Thr Leu Pro Tyr Phe Ala Ile Met Thr Ile Phe Ser Gly Phe Asn 20 25 30 Tyr Val Leu Ile Asn Phe Leu Thr Asn Pro Ser Phe Tyr Asn Ile Pro 35 40 45 Thr Ala Arg Ile Leu Ile Asp Ile Leu Ile Phe Gly Phe Ile Leu Ile 50 55 60 Ser Leu Leu Met Leu Leu Tyr Gly Arg Tyr Ala Asn Arg Phe Ile Ser 65 70 75 80 Asp Glu Arg Asn Ser Asn Met Gly Ile Phe Leu Met Leu Gly Met Gly 85 90 95 Lys Lys Gln Leu Leu Lys Ile Ile Tyr Leu Glu Lys Leu Tyr Leu Phe 100 105 110 Thr Gly Thr Phe Phe Gly Gly Leu Ile Phe Gly Phe Val Tyr Ser Lys 115 120 125 Ile Phe Phe Leu Phe Ile Arg Asn Leu Ile Val Ile Gly Asp Val Arg 130 135 140 Glu Gln Tyr Ser Leu Thr Ala Ile Ser Trp Leu Leu Ile Leu Thr Phe 145 150 155 160 Phe Ile Tyr Phe Ile Ile Tyr Leu Ser Glu Tyr Arg Leu Leu Lys Arg 165 170 175 Gln Ser Ile Thr Val Ile Phe Asn Ser Lys Ala Lys Arg Asp Asn Pro 180 185 190 Arg Lys Thr Ser Val Phe Val Gly Leu Phe Gly Leu Phe Ala Leu Leu 195 200 205 Met Gly Tyr His Phe Ala Leu Thr Ser Pro Asn Val Thr Thr Ser Phe 210 215 220 Ser Arg Phe Ile Tyr Ala Ala Cys Leu Val Thr Leu Gly Ile Phe Cys 225 230 235 240 Thr Phe Ser Ser Gly Val Ile Met Leu Leu Thr Val Ile Lys Lys Arg 245 250 255 Arg Ala Ile Tyr Tyr Asn Gln Arg Arg Phe Val Val Ile Ala Ser Leu 260 265 270 Phe His Arg Ile Arg Ser Asn Ala Leu Ser Leu Ala Thr Ile Cys Ile 275 280 285 Phe Ser Thr Ala Thr Leu Val Ser Leu Ser Val Leu Ala Ser Leu Tyr 290 295 300 Leu Ala Lys Asp Asn Met Val Arg Leu Ser Ser Pro Arg Asp Val Thr 305 310 315 320 Val Leu Ser Thr Thr Asp Ile Glu Pro Asn Leu Met Asp Ile Ala Thr 325 330 335 Lys Asn His Val Thr Leu Thr Asn Arg Gln Asn Leu Lys Val Ser Gln 340 345 350 Ser Val Tyr Gly Asn Ile Lys Gly Ser His Leu Ser Val Asp Pro Asn 355 360 365 Gly Gly Met Ala Asn Asp Tyr Gln Ile Thr Val Ile Ser Leu Asp Ser 370 375 380 Phe Asn Ala Ser Asn Asn Thr His Tyr Arg Leu Lys Asn His Glu Ile 385 390 395 400 Leu Thr Tyr Val Ser Asn Gly Ala Ala Ala Pro Ser Ser Tyr Thr Thr 405 410 415 Asn Gly Val Lys Leu Thr Asn Val Lys Gln Ile Lys Arg Ile Asn Phe 420 425 430 Ile Phe Ser Pro Leu Arg Ser Met Gln Pro Asn Phe Phe Ile Ile Thr 435 440 445 Asp Asn Arg Glu Ile Ile Gln Thr Ile Leu Lys Glu Glu Leu Thr Trp 450 455 460 Gly Thr Met Ala Gly Tyr His Val Lys Gly Lys Lys Met Asn Gln Lys 465 470 475 480 Asp Phe Tyr Asp Glu Leu Glu Thr Thr Asn Phe Arg Gln Phe Ser Ala 485 490 495 Asn Val Val Ser Ile Arg Gln Val Lys Ser Met Phe Asn Ala Leu Phe 500 505 510 Gly Gly Leu Leu Phe Val Gly Ile Ile Phe Gly Thr Ile Phe Ala Ile 515 520 525 Leu Thr Ala Ile Thr Ile Tyr Tyr Gln Gln Leu Ser Glu Gly Ile Arg 530 535 540 Asp Arg Asp Asp Tyr Lys Ala Met Ile Lys Leu Gly Met Thr Asn Lys 545 550 555 560 Thr Ile Gln Asp Ser Ile Lys Val Gln Ile Asn Phe Val Phe Ile Leu 565 570 575 Pro Ile Ala Phe Ala Leu Leu Asn Leu Ile Phe Ala Leu Pro Ile Leu 580 585 590 Tyr Lys Ile Met Thr Thr Phe Gly Phe Asn Asp Ala Gly Leu Phe Leu 595 600 605 Arg Ala Val Gly Thr Cys Leu Ile Val Tyr Leu Phe Phe Tyr Trp Phe 610 615 620 Ile Cys His Cys Thr Ser Lys Leu Tyr Tyr Arg Leu Ile Ser Lys Lys 625 630 635 640 17 118 PRT Streptococcus mutans 17 Met Arg Ile Val Ser Ser Leu Val Ser Leu Leu Leu Thr Ile Phe Trp 1 5 10 15 Ile Phe Ala Ile Ala Phe Ile Pro Ile Gly Asp Gln Asn Ser Phe Asn 20 25 30 Lys Pro Glu Met Trp Phe Phe Val Phe Phe Ala Ile Ile Ile Tyr Ser 35 40 45 Ile Val Ile Ile Ser Asp Tyr Tyr Leu Lys Ser Phe Asn Leu Leu Lys 50 55 60 Val Tyr Gln Ile Leu Val Leu Phe Ile Ser Ile Leu Cys Ala Leu Cys 65 70 75 80 Gly Leu Ser Leu Thr Ala Leu Gly Leu Lys Val Phe Thr Leu Ala Ile 85 90 95 Gly Ile Val Ser Leu Val Asn Thr Ile Ile Tyr Phe Phe Phe Ala Asn 100 105 110 Lys Lys Asp Asn Val Glu 115 

1. A purified and isolated nucleic acid sequence coding for a lantibiotic as set forth in SEQ ID No:
 1. 2. A vector which comprises the nucleic acid of claim
 1. 3. A prokaryotic or eukaryotic host cell transformed or transfected with the vector of claim
 2. 4. An isolated and purified DNA sequence comprising a protein coding sequence encoding the expression of the protein of SEQ ID No:
 2. 5. An isolated and purified peptide sequence having an amino acid sequence for a antibiotic as set forth in SEQ ID No: 2, or a pharmaceutically acceptable salt, ester, amide, and prodrug thereof.
 6. A method of making mutacin I protein comprising culturing a microorganism transformed with DNA (SEQ ID No: 1) encoding for mutacin I protein and recovering mutacin I protein.
 7. A method according to claim 6, wherein said culturing step comprises disposing the microorganisms on a membrane.
 8. A method according to claim 7 wherein said culturing step comprises contacting the membrane having the microorganism thereon with a growth media.
 9. A method according to claim 8, further comprising the step of freezing the growth media having the microorganism thereon and then thawing the growth media.
 10. A method according to claim 9, further comprising the step of separating a liquid fraction of the growth media from a solid fraction of the growth media.
 11. A method according to claim 10, wherein said recovery step comprises the step of chromatographically separating the mutacin I from the liquid fraction.
 12. A process for the production of mutacin I having part or all of the primary structural conformation and biological activity of bacterial mutacin I, said process comprising: growing, under suitable conditions, prokaryotic or eukaryotic host cells transformed or transfected with a DNA sequence according to claim 1 in a manner allowing expression of said mutacin I product; and isolating the mutacin I product of the expression of said DNA sequence.
 13. A mutacin I protein product of the expression in a prokaryotic or eukaryotic host cell of DNA according to claim
 12. 14. A method of treating or preventing an infection in a subject, said method comprising administering to said subject an effective amount of a purified and isolated peptide having the amino acid sequence as set forth in SEQ ID No: 2, or a pharmaceutically acceptable salt, amide, ester, or prodrug thereof.
 15. A method according to claim 14, wherein the pep tide is administered orally.
 16. A method according to claim 14, wherein the peptide is administered topically.
 17. A method according to claim 14, wherein the peptide is applied to a surface of a medical device.
 18. A method according to claim 17, wherein the medical device is a catheter.
 19. A method according to claim 17, further including the step of coating the medical device with the peptide prior to contacting the subject therewith.
 20. A pharmaceutical composition comprising a peptide having amino acid sequence SEQ ID No: 2 and a pharmaceutically acceptable carrier. 